UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

WASHINGTON, D.C. 20549

FORM 10-K

(Mark One)

x
ýANNUAL REPORT UNDER SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934.

For the fiscal year ended June 30, 20122015

¨TRANSITION REPORT UNDER SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934.

For the transition period from                      to                     

Commission file number: 000-30489001-35647

LIFEVANTAGE CORPORATION

(Exact name of registrant as specified in its charter)

Colorado90-0224471

(State or other jurisdiction of

incorporation or organization)

(IRS Employer
Identification No.)
 

(IRS Employer

Identification No.)

98159785 S. Monroe, Ste 100300
Sandy, UT 8407084070
(Address of principal executive offices)offices, including zip code)
 
(Zip Code)Registrant’s telephone number: (801) 432-9000

Registrant’s telephone number: (801) 432-9000

Securities registered pursuant to Section 12(b) of the Act: None

Securities registered pursuant to Section 12(g) of the Act:

Common Stock, $0.001 par value per share

(Title of Class)

Indicate by check mark if the registrant is a well-known seasoned issuer, as defined in Rule 405 of the Securities Act.    Yes  ¨    No  xý

Indicate by check mark if the registrant is not required to file reports pursuant to Section 13 or Section 15(d) of the Act.    Yes  ¨    No  xý

Indicate by check mark whether the registrant (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filing requirements for the past 90 days.    Yes  xý    No  ¨

Indicate by check mark whether the registrant has submitted electronically and posted on its corporate Web site, if any, every Interactive Data File required to be submitted and posted pursuant to Rule 405 of Regulation S-T during the preceding 12 months (or for such shorter period that the registrant was required to submit and post such files).    Yes  xý    No  ¨

Indicate by check mark if disclosure of delinquent filers pursuant to Item 405 of Regulation S-K is not contained herein, and will not be contained, to the best of registrant’s knowledge, in definitive proxy or information statements incorporated by reference in Part III of this Form 10-K or any amendment to this Form 10-K.  ¨

Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, or a smaller reporting company. See the definitions of “large accelerated filer,” “accelerated filer” and “smaller reporting company” in Rule 12b-2 of the Exchange Act. (Check one):

Large accelerated filer¨Accelerated filerx
ý
Non-accelerated filer
¨ (Do not check if a smaller reporting company)
Smaller reporting company¨

Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Act).    Yes  ¨    No  xý

The aggregate market value of the registrant’sregistrant's common stock (par value $0.001) held by non-affiliates as of December, 31, 2014, the end of the registrant’sregistrant's second fiscal quarter, December 31, 2011, was $143 million. Sharesapproximately $128.5 million, based on a closing market price of the registrant’s common stock held by each current executive officer and director and by each shareholder who is known by the registrant to own 10% or more of the outstanding common stock have been excluded from this computation in that such persons may be deemed to be affiliates of the registrant. Share ownership information of certain persons known by the registrant to own greater than 10% of the outstanding common stock for purposes of the preceding calculation is based solely on information on Schedules 13D and 13G, if any, filed with the Commission. This determination of affiliate status is not necessarily a conclusive determination for other purposes.

$1.30 per share.

The number of shares of common stock (par value $0.001) outstanding as of August 30, 2012,27, 2015, was 111,156,20197,537,215 shares.

DOCUMENTS INCORPORATED BY REFERENCE

Portions of the registrant’s definitive proxy statement to be filed subsequent to the date hereof with the Securities and Exchange Commission pursuant to Regulation 14A in connection with the registrant’s fiscal year 20132015 annual meeting of shareholders are incorporated by reference into Part III of this report. Such definitive proxy statement will be filed with the Commission not later than 120 days after the end of the registrant’s fiscal year ended June 30, 2012.

2015.





CAUTIONARY NOTE REGARDING FORWARD-LOOKING STATEMENTS

Certain statements contained in this report and the information incorporated by reference herein may contain “forward-looking statements” (as such term is defined in Section 27A of the Securities Act of 1933, as amended and Section 21E of the Securities Exchange Act of 1934, as amended). These statements, which involve risks and uncertainties, reflect our current expectations, intentions, or strategies regarding our possible future results of operations, performance, and achievements. Forward-looking statements include, without limitation: statements regarding future products or product development; statements regarding future selling, marketing, general and administrative costs and research and development spending; statements regarding expansion in new and existing markets; statements regarding our product development strategy; statements regarding the future performance of our network marketing sales;business; and statements regarding future financial performance and results of operations. These forward-looking statements are made pursuant to the safe harbor provisions of the Private Securities Litigation Reform Act of 1995, and applicable rules of the Securities and Exchange Commission and common law.

These forward-looking statements may be identified in this report and the information incorporated by reference by words such as “anticipate”, “believe”, “could”, “estimate”, “expect”, “intend”, “plan”, “predict”, “project”, “should” and similar terms and expressions, including references to assumptions and strategies. These statements reflect our current beliefs and are based on information currently available to us. Accordingly, these statements are subject to certain risks, uncertainties, and contingencies, which could cause our actual results, performance, or achievements to differ materially from those expressed in, or implied by, such statements.

The following factors are among those that may cause actual results to differ materially from our forward-looking statements:

Inability to successfullystrengthen our business and properly manage distractions among our distributors in Japan;

Inability to manage existing markets, open new international markets or expand our operations in both existingoperations;
Inability of new products to gain distributor or market acceptance;
Our inability to execute our product launch process due to increased pressure on our supply chain, information systems and new markets;

management;

Difficulty in managing our growth and expansion;

Inability to conform to government regulations in Japan;

Disruptions in our information technology systems;

Inability to comply with financial covenants imposed by our credit facility;

Inability to protect against cyber security risks and to maintain the integrity of data;
The impact of our debt service obligations and restrictive debt covenants;
Claims against us as a result of our independent distributors failing to comply with applicable legal requirements or our policies and procedures;
International trade or foreign exchange restrictions, increased tariffs, foreign currency exchange;
Deterioration of global economic conditions and the decline of consumer confidence and spending;

conditions;

We may need to raise additional capital;

Environmental liabilities stemming from past operations and property ownership;

Inability to maintain appropriate level of internal control over financial reporting;

Inability to raise additional capital if needed;

Exposure to environmental liabilities stemming from past operations and property ownership;
Significant dependence upon a single product;

product for revenue;

Improper actions by our independent distributors that violate laws or regulations;

Our abilityInability to retain independent distributors or to attract new independent distributors on an ongoing basis;

CompetitionHigh quality material for our products may become difficult to obtain or expensive;

Improper actions by our independent distributors that violate laws or regulations;
Dependence on third parties to manufacture our products;
Disruptions to the transportation channels used to distribute our products;
We may be subject to a product recall;

- 2-



Government regulations on direct selling activities may prohibit or severely restrict our business model;
Unfavorable publicity on our business or products;
Our direct selling program could be found to not be in the dietary supplement market;

compliance with current or newly adopted laws or regulations;

Legal proceedings may be expensive and time consuming;

Strict government regulations on our business;
Regulations governing the production or marketing of our personal care product;

products;

Significant government regulations on network marketing activities;

Our business is subject to strict government regulations;

Unfavorable publicity on our business or products;

Our inability to protect our intellectual property rights;

Third party claims that we infringe on their intellectual property rights;

-2-


We are subject to the riskRisk of investigatory and enforcement action by the federal trade commission;

Government authorities may question our tax positions or transfer pricing policies or change their laws in a manner that could increase our effective tax rate or otherwise harm our business;

Failure to comply with anti-corruption laws;
Inability to build and integrate our new management team could harm our business;
Loss of, or inability to attract, key personnel;
We could be held responsible for certain taxes or assessments relating to the activity of our independent distributors;
Competition in the dietary supplement market;
Our inability to protect our intellectual property rights;
Third party and governmental actions involving our network marketing sales activities;

Our dependenceclaims that we infringe on third party manufacturers to manufacture our product;

their intellectual property;

Our ability to obtain raw material for our product;

Product liability claims against us;

Loss of key personnel;

Economic, political, foreign exchange and other risks associated with international operations;

Our inability to regain compliance with the Nasdaq Capital Market continued listing standards;

Volatility of the market price of our common stock;
Substantial sales of shares may negatively impact the market price of our common stock;
Significant dilution of outstanding voting shares if holders of our existing warrants and options exercise their securities for shares of common stock;

and

The market price of our securities could be adversely affected by the sales of restricted securities;

Volatility of the market price of our common stock;

The illiquidity of our common stock;

Substantial sales of shares of our common stock; and

We have not paid dividends on our capital stock, and we do not currently anticipate paying dividends in the foreseeable future.

When considering these forward-looking statements, you should keep in mind the cautionary statements in this report and the documents incorporated by reference. Except as required by law, we have no obligation and do not undertake to update or revise any such forward-looking statements to reflect events or circumstances after the date of this report.

-3-


- 3-



TABLE OF CONTENTS

 Page
Page 
PART I

21

31

31

31

31 
PART II

32

32

33

38

38

38

38

39 
PART III

40

40

40

40

40 
PART IV

41

42

-4-


- 4-



PART I

ITEM 1 — BUSINESS

Overview

LifeVantage Corporation is a company dedicated to helping people achieve their health, wellness and financial independence goals. We provide quality, scientifically validatedscientifically-validated products and a financially rewarding network marketing business opportunity to customers and independent distributors who seek a healthy lifestyle and financial freedom. We sell our products in the United States, Japan, Hong Kong, Australia, Canada, Philippines, Mexico and Mexico through a network of independent distributors, and to preferred and retail customers. We also sell our products directly to consumers located in Canada for personal consumption.

Thailand.

We engage in the identification, research, development manufacture and distribution of advanced nutraceutical dietary supplements and skin care products, including our flagship product, Protandim®, the Nrf2 Synergizerour scientifically-validated dietary supplement, LifeVantage TrueScience®and, our line of revolutionary anti-aging skin care product, LifeVantage TrueScienceproducts, Canine Health®. We currently focus, our ongoing internal research efforts oncompanion pet supplement formulated to combat oxidative stress solutions, particularly the activation of Nuclear factor (erythroid-derived 2)-like 2, also known as Nrf2, as it relates to health-related disorders.in dogs, and Axio

®, our energy drink mixes.

We were incorporated in Colorado in June 1988 under the name Andraplex Corporation. We changed our corporate name to Yaak River Resources, Inc. in January 1992, and subsequently changed it again in October 2004 to Lifeline Therapeutics, Inc. In October 2004 and March 2005, we acquired all of the outstanding common stock of Lifeline Nutraceuticals Corporation, our wholly-owned subsidiary through which we hold the patent rights relating to Protandim® and other intellectual property.Corporation. In November 2006, we changed our name to LifeVantage Corporation.

LifeVantage Corporation, the LifeVantage Corporation logo, LifeVantage®, Protandim®, the Nrf2 Synergizer and LifeVantage TrueScience are trademarks of LifeVantage Corporation in the United States and in other selected countries. All other brand names or trademarks appearing in this report are the property of their respective holders. Unless otherwise noted, the terms “we”, “our”, “us”, the “Company” and “LifeVantage” refer to LifeVantage Corporation.

Recent Developments

As part of our substantial growth since beginning to sell our products through network marketing in 2009, we have sought to build a well-disciplined management team that focuses on strategic and tactical delivery of our products and business opportunities to our independent distributors and customers. During From our fiscal year 2012,2005 until our fiscal year 2009, we added key membersmarketed and sold a single product, Protandim®, through traditional retail stores. In October 2008, we announced that we were transitioning our business model from a traditional retail model to a network marketing model in which Protandim® would be sold primarily through our network of independent distributors. Since entering network marketing, we have increased our geographic reach by entering new international markets and increased our product offering by introducing additional scientifically-validated products.

Fiscal Year 2015 Highlights
We expanded our product offering in October 2014 by introducing Axio®, our energy mixes. Axio® is formulated to promote alertness and support mental performance. We currently have additional products in development. We intend to conduct additional research and development on these and other product candidates before introducing them through our network of independent distributors. We believe these new product lines, together with Protandim®, show our commitment to delivering scientifically backed products that help people feel, look and perform better.
We commenced our partnership with Real Salt Lake of Major League Soccer in January 2014. Our partnership with Real Salt Lake includes placement of our logo on the front of the team's jersey as well as strategic placement of our logo around the stadium and on televised broadcasts of games. During fiscal 2015, we expanded this partnership by hosting distributor recruiting events at Real Salt Lake games in the U.S. and Canada. We believe the partnership provides the LifeVantage brand with high-impact exposure and recognition in stadiums, on television, in advertising and through player appearances across the country and around the world.
We made significant changes to our executive management team includingduring fiscal year 2015. Most significantly, in May 2015, we appointed Darren Jensen as our President and Chief Executive Officer. Prior to joining LifeVantage, Mr. Jensen has spent his entire career in the direct selling industry. Most recently, he served as President-Americas beginning in June 2014 and prior to that, Chief Sales Officer from September 2012 to June 2014 at Jeunesse Global, a personal care and nutrition direct selling company. Prior to Jeunesse, Mr. Jensen served as Chief OperatingSales Officer General Counsel andat Ampegy, a direct selling company focused on the energy industry. Prior to Ampegy, Mr. Jensen served as Executive Vice President of Marketing and Communications.

During fiscal 2012, we increased our international expansion efforts, including significantly increasing sales in Japan, shipping products for personal consumption to customers in Canada and opening the market of Australia to our independent distributors and preferred customers. In addition, on May 14, 2012, the USPTO allowed the issuance of U.S. Patent Application No. 13/039,073, Compositions for Alleviating Inflammation and Oxidative Stress inCorporate General Manager at Agel Enterprises, a Mammal. Our fifth patent, Patent No. 8,221,805, was issued therefrom on July 17, 2012.

nutritional supplements direct selling company.

Our Competitive Advantage

Advantages

We believe that we offerhave a competitive advantage in several key areas:

Our Business Opportunity: We offer a plan to our independent distributors that enables them to earn compensation early, frequently and consistently

Our Compensation: We believe our compensation plan is one of the more financially rewarding in the direct selling industry. Our percentage of sales paid to independent distributors as compensation and incentive is one of the highest percentages reported in the direct selling industry. Our compensation plan also enables independent distributors to earn compensation early and often as they sell our products. Some elements of our compensation plan are paid weekly, allowing new independent distributors to receive compensation quickly. We believe more frequent payments of compensation helps us retain new independent distributors by allowing them to experience success soon after enrolling. We also offer a variety of incentive programs to our independent distributors for achieving specified sales goals. For example, our My LifeVentures® is an incentive program that enables independent distributors to earn the title to a new Jeep Wrangler by achieving and maintaining specified sales goals. We also offer various training

- 5-



resources to help our independent distributors become more effective. We believe our compensation plan, is one of the most rewarding in the industry. Our compensation plan is structuredincentive programs and training resources help to allow new,

motivate and prepare our independent distributors for success.

-5-


inexperienced independent distributors to succeed early and to achieve residual income at all levels of their business. We believe these factors lead to increased sales of our products by allowing us to attract and retain leaders in our independent distributor ranks and to create leaders out of previously inexperienced independent distributors.

Our Products: We offer revolutionaryquality, scientifically-validated products focused on healthy living that are backed by numerous scientific studies. Ourhelping individuals look, feel and perform better. Protandim® product is a patented dietary supplement that has been clinically proven to combat oxidative stress, which refers to the cellular and tissue damage that occurs as a natural consequence of aging and disease. Protandimcellular metabolism associated with many of the undesirable effects of aging. Our skin care line, LifeVantage TrueScience® has also been studied extensively in the laboratory and is the subject of eleven peer-reviewed publications discussing the breadth of its efficacy and safety. Our skincare cream, LifeVantage TrueScience®, is a unique,combination of scientifically based anti-aging skin care product.products formulated to target the visible signs of aging on the skin. Axio®, introduced in November 2014, is our new line of energy drink mixes formulated to promote alertness and support mental performance. Our companion pet supplement, Canine Health®, incorporates some of the same active ingredients as Protandim® to combat oxidative stress in dogs. We intend to continuebelieve our research and development efforts on our current products to further validate the benefits they provide. In addition, as we pursue the development and acquisition of additional products, we intend to maintain our focus on providing unique, scientifically validated and high-quality products for our independent distributors and customers to sell and use. Unlike other network marketing companies, we have a substantialsignificant number of “preferred customers”preferred customers who regularly purchase our products even though they do not intend to becomewithout the intention of becoming independent distributors. This representsdistributors is a diversified sourcestrong indicator of revenue, beyond that generated solely from sales tothe benefits of our independent distributors.products.

Our Method: We offer a variety of compelling rewards and incentives to our independent distributors for achieving specified sales and education goals. In addition, we offer a robust training program that teaches and trains our independent distributors how to become successful with their entrepreneurial goals and to do so in compliance with all of our policies and procedures. We also routinely provide the opportunity for independent distributors to be recognized as leaders and for their other success at a variety of global events that we sponsor. These rewards, training and recognition programs enhance our independent distributors’ opportunities for success and lead to increased sales of our products to consumers.

Our Culture: We are committed to creating a culture for our independent distributors and employees that focuses on ethical, legal and transparent business practices. We have developed a system ofAt enrollment, our independent distributors agree to abide by our policies and procedures. Our policies and procedures, forwhen followed, ensure that our independent distributors to follow that enables them to be maximally effectivecomply with applicable laws and compliant with laws. We monitorregulations. Our compliance department monitors the activities of our independent distributor activity in each marketdistributors as part of our effortseffort to enforce our policies and procedures and systematically review and act on reports of alleged independent distributor misbehavior with our internal compliance department.procedures. Similarly, our code of business conduct and ethics sets forth principals to guideguidelines and expectations for our employees and encourage them to avoid any appearance of improper behavior.employees. We believe that by encouraging a positive, goal –orientedour ethical, legal and ethicaltransparent culture we will be able to attractattracts highly qualified employees and independent distributors.

distributors who share our commitment to these principles.

Our Employees: We believe that our employees are an essential asset. We have a dedicated team of professionals that support our system of independent distributors, work to generate long-term value for our shareholders and contribute to the broader public through LifeVantage Legacy and other charitable programs. In turn, we offer competitive compensation, invest in our employees' careers and direct their focus on the long-term goals of our independent distributors and shareholders.
Scientific Background

Oxidative Stress

Oxidative stress refers to the cellular and tissue damage caused by chemically reactive oxygen radicals and related oxidants, formedspecies that is generated as a natural consequenceresult of cellular metabolism and which results from the body's use of oxygen to generate energy. A small percentage of the oxygen we utilize generates toxic oxygen free radicals that damage human cells and tissue and consequently negatively impact our general health. Levels of these reactive oxygen species, also known as ROS, and free radicals can be elevated under a wide variety of conditions, including radiation, UV light, smoking, excessive alcohol consumption, as well as medical conditions involving inflammation, cardiovascular disease, neurodegenerative disease, diabetes and advancing age.

Elevated ROS levels inflict structural damage toon nucleic acid, lipid, carbohydrate and protein components of cells, thereby directly contributing to or exacerbating tissue dysfunction, disease and age-related debilitation. Normally, cellular

Cellular antioxidant enzymes normally serve to inactivate ROS and maintain their levels of ROS at those compatible with normal cell function. Important among these cellular antioxidant enzymes are superoxide dismutase and catalase. However, the levels of these protective antioxidant enzymes decrease with age and also decrease in a number of disease conditions, while ROSconditions. As we age and the levels may increase.

-6-


Superoxide dismutase is believed to be the body’s most effective natural antioxidant. Superoxide dismutase works in conjunction with catalase and under some circumstances the balance between these two enzymes may be important. The potent antioxidant activity of superoxide dismutase produces hydrogen peroxide, as a by-product, a dangerous substance that subsequently needs to be converted into water and oxygen by catalase. Together, these two enzymes constitute the first line of antioxidant defense in humans. Scientists have long believed that increasing levels of superoxide dismutase and catalase is an important means of fighting oxidative stress, disease, and the effects of aging; however, superoxide dismutase and catalase supplements by themselves have not been shown to be absorbed and retain activity when taken by oral administration.

Oxidative stress is the result of the metabolic process and may promote some of the undesirable effects of aging. As the body ages,enzymes decrease, oxidative stress levels increase significantly as theand our body is unable to maintain homeostasis relative to the free radicals produced through the metabolic process.

elevated ROS levels.

Oxidative stress is widely believed to be a key factor in many of the undesirable effects of aging process by triggering prematurebecause it promotes cell death. The body’s defenses against oxidative stress and free radicals decrease with age. HighAdditionally, high levels of oxidative stress hashave also been linked as a causative or associated factor in over 100 diseases, including cancer, cardiovascular diseases, inflammation, neurological diseases and renal disease, and, conversely, lowering oxidative stress levels is linked to improved health.

diseases.

Nrf2 Activation

Nuclear factor (erythroid-derived 2)-like 2, also known as NFE2L2 or Nrf2, is a transcription factor that in humans is encoded by the NFE2L2 gene. Nrf2 is the master regulator of the antioxidant response, which is important for the amelioration of oxidative stress. Oxidative stress is a causative factor in cancer, cardiovascular diseases, inflammation, neurological diseases and renal disease. Because Nrf2 is able to induce gene activity important in combating oxidative stress, thereby activating the body’s own protective response, it helps protect from a variety of complications related to oxidative stress.

Under normal or unstressed conditions, Nrf2 resides in the cytoplasm of the cell, outside the nucleus.nucleus, and is targeted for degradation. When activated, Nrf2 is able to move into the nucleus, where it promotes the expression of several thousand genes, including those that encode antioxidant enzymes as well as anti-inflammatory and anti-fibroticstress response proteins. These include, but are not limited to, the following:

NAD(P)H quinone oxidoreductase 1 (Nqo1), a Nrf2 target gene that catalyzes the reduction and detoxification of highly reactive quinones that can cause redox cycling and oxidative stress.

Glutathione synthase and xCT, a protein required for cystine amino acid entry into the cell, which establish Nrf2 as a regulator of glutathione, one of the most important antioxidants in the body.

Heme oxygenase-1 (HMOX1), an enzyme that catalyzes the breakdown of heme into the antioxidant biliverdin, the anti-inflammatory agent carbon monoxide, and iron. HO-1 is a Nrf2 target gene that has been shown to protect from a variety of pathologies, including sepsis, hypertension, atherosclerosis, acute lung injury, kidney injury and pain.

The glutathione S-transferase (GST) family, including cytosolic, mitochondrial and microsomal enzymes that catalyze the conjugation of GSH with a number of toxic molecules, aiding in their elimination from the body.

Nrf2 as a therapeutic target

In recent years, Nrf2 has become the subject of intense research. A common theme in much of this research is that activation of Nrf2 upregulates a coordinated antioxidant response and is therefore capable of protecting against oxidative


- 6-



stress-related injury and inflammatory disease in a wide variety of animal models. Therefore, Nrf2 represents a novelan important therapeutic target.

-7-


Research and Development

We believe thatHistorically, we have focused our research and development efforts to date related to ouron creating and supporting scientifically-validated, yet highly demonstrative products under the Protandim® and LifeVantage, TrueScience® products are one, Canine Health®, and Axio® federation of brands. We anticipate that our most important competitive strengths. We intend to further expand ourfuture research and development efforts to create and/or develop additionalwill be focused on creating, developing and evaluating new products that combatare consistent with our commitment to provide quality, scientifically-validated products. We intend to build on our foundation of combating oxidative stress orand targeting specific benefit areas that otherwise have strong scientific background or potential.help individuals feel, look and perform better, including exploring products focused on weight-loss and gut health. We also plan to continue sponsoring additional studies on our current products in an effort to further validate the benefits they provide.

Product Overview
Protandim

®

Protandim®

Our Protandim® product is a patented dietary supplement that has been shown in a clinical trial to reduce the age-dependent increase in markers of oxidative stress, and has also been shown to provide substantial benefits to combat the variety of negative health effects linked to oxidative stress.

Protandim® combats oxidative stress by increasing the body’s natural antioxidant protection at the genetic level, inducing the production of naturally-occurring protective antioxidant enzymes including superoxide dismutase, catalase, and glutathione synthase.level. The unique blend of phytonutrients in Protandim® signals the activation of Nrf2 to increase production of antioxidant enzymes, specifically superoxide dismutase and catalase, and other stress-relatedcell-protective gene products. TheseThe body's internally produced antioxidant enzymes provide a better defense against oxidative stress than externally derived sources of antioxidants such as Vitamin C, Vitamin E and Coenzyme Q-10. Unlike externally derived sources of antioxidants, these enzymes are “catalytic,” which means thatthese enzymes such as superoxide dismutase and catalase are not used up when they neutralizeupon neutralizing free radicals.

Nrf2 decreases the expression of many pro-inflammatory

We hold six U.S. and pro-fibrotic genes. Inflammation accompanies many diseases including arthritis, but inflammation also occurs with traumatic injuries, such as cuts, sprains or bruises. The process of inflammation is designed, in part, to prevent infection by killing foreign microorganisms through the creation of toxic free radicals. Thus the pain, redness and swelling associated with a disease or injury are largely due to inflammation as the body responds (or over responds) to the threat of infection. With many diseases or traumatic injuries, inflammation is followed by scar tissue formation, referred to as fibrosis.

We held fourfive international patents relating to our Protandim® product as of June 30, 2012, and a fifth patent relating to our Protandim® product was granted in July 2012.. We believe these patents set Protandim® apart from other dietary supplements and protect the original formula as well as certain formula modifications we could create to extend our Protandim® product line. We sell Protandim

Protandim® in two formulas, one for the Japan market and the other formula for all other markets.

Protandim® has been, orand is currently, the subject of numerous independent scientific studies at various universities and research facilities.facilities including The nature and stages of the studies vary, as some are still in planning stages, while other studies are in progress or completed. The universities and institutions involved in this research include theOhio State University, Louisiana State University, University of Colorado;Colorado Denver, Virginia Commonwealth University, Colorado State University; Children’s Hospital, Denver; Virginia Commonwealth University; Louisiana State University; Ohio State University; Northwestern University; Medical CollegeUniversity and Texas Tech University. The results of Wisconsin; Harvard University; and VU University Medical Center, Amsterdam. The various studies deal with the alleviation of oxidative stress under the following conditions: altitude sickness, alcoholic and non-alcoholic steatohepatitis, lung antioxidant status in withdrawing alcoholics, autonomic physiology and aging, skin cancer, multiple sclerosis, pulmonary hypertension, heart disease, coronary artery bypass graft failure, Duchenne muscular dystrophy, and salt-sensitive hypertension.

Clinical Study

A peer-reviewed human clinical study that we conducted in 2004 and 2005 showed that after Protandim® was taken for 30 consecutive days, the level of circulating TBARS, a laboratory marker for oxidative stress in the human body, decreased by an average of 40 percent, to levels typical to a 20-year-old. When taken for 120

consecutive days, Protandim® increased the activity of superoxide dismutase and catalase antioxidant enzymes by up to 54 percent, substantially increasing the body’s antioxidant defenses. This study was published in the journalFree Radical Biology and Medicine, vol. 40, pp. 341-7 (2006).

-8-


Published Peer Reviewed Studies and Papers

Since the initial clinical studies completed in 2004 and 2005, Protandim® has been studied and reviewed in numerous laboratories of respected universities and institutions. Pre-clinicalthese studies have been published in a variety of peer-reviewed scientific journals, including: a study that we funded which explored the synergistic mechanism of action of Protandimincluding ®; an animal study using mice to examine the tumor prevention capabilities of Protandim® conducted at Louisiana State University; an animal study exploring pulmonary hypertension and subsequent right heart failure conducted at Virginia Commonwealth University; an animal study examining the effects of Protandim® in a mouse model of Duchenne Muscular Dystrophy conducted at the University of Colorado; a second study conducted at Louisiana State University probing Protandim®’s ability to modulate the relationship between superoxide dismutase and tumor suppressor p53; a study conducted at The Ohio State University showing that Protandim® markedly decreases the intimal hyperplasia (or wall thickening) of saphenous veins, as occurs when such veins are used in coronary artery by-pass grafting; a Company-funded study which examined Protandim®’s effects on gene expression relative to colon carcinoma, atherosclerosis, and Alzheimer’s disease; and a study conducted at Colorado State University demonstrating effects of Protandim® on human coronary artery endothelial cells and resistance to oxidative stress in vitro.

The mechanism of action for Protandim® was discovered to be activation of the transcription factor Nrf2 in a study we funded, the results of which were subsequently published in February 2009. This study also demonstrated synergy among the five active ingredients of Protandim® which would enable them to be effective while being administered at lower concentrations of each. This peer-reviewed study was published inFree Radical Biology and& Medicine, vol. 46, pp. 430-40 (2009).

A study completed at Louisiana State University and sponsored by the Skin Cancer Foundation was published in theEnzyme Research, Circulation-the scientific journalPloS ONE,vol. 4: e5284 (2009), an international, peer-reviewed, open access journal published by the Public Library of Science. This study, entitled “Protandim®, a Fundamentally New Antioxidant Approach in Chemoprevention Using Mouse Two-Stage Skin Carcinogenesis as a Model,” investigated whether Protandim® could suppress tumor formation in mice through a dietary approach. At the end of a two-stage skin carcinogenesis, the mice on the Protandim®-supplemented diet showed a reduction in both skin tumor incidence and multiplicity by 33% and 57% respectively, compared to those that did not receive Protandim® supplementation.

A study at Virginia Commonwealth University study was published inCirculation, vol. 120, pp. 1951-1960 (2009),a journal published by the American Heart Association. This study, entitled “Chronic Pulmonary Artery Pressure Elevation Is Insufficient to Explain Right Heart Failure,” investigated the abilityAssociation, American Journal of Protandim® to protect the heart in a laboratory model of pulmonary hypertension in rats. The researchers concluded that Protandim® prevented the death of heart cells in ratsPhysiology-Lung Cellular and significantly lowered osteopontin (OPN-1) levels by more than 50%, and that Protandim® effectively activated the transcription factor Nrf2, a signal to the cell’s DNA to increase expression of a network of antioxidants, anti-inflammatory, and anti-fibrotic genes.

The study,The Dietary Supplement Protandim® Decreases Plasma Osteopontin and Improves Markers of Oxidative Stress in Muscular Dystrophy Mdx Mice, was published in theMolecular Physiology, PLoS One, Journal of Dietary Supplements, vol. 7: 159-78 (2010), and concluded that Protandim® caused a decrease in the production of the pro-fibrotic gene product osteopontin. It also concluded that Protandim® decreases markers of lipid peroxidation in a model of Duchenne Muscular Dystrophy (DMD). The study was published by Dr. Brian Tseng and his colleagues at Massachusetts General Hospital, Harvard Medical School, and the University of Colorado Denver.

Another study, titled“The Chemopreventive Effects of Protandim®: Modulation of p53 Mitochondrial Translocation and Apoptosis during Skin Carcinogenesis,” was conducted by researchers at Louisiana State University and published in the scientific journalPloS ONE, vol. 5: e11902 (2010). This study further investigated Protandim®’s ability to increase production of Nrf2-regulated protective genes. This study examined the biochemical mechanisms that underlie the ability of Protandim® to suppress tumors in mice.

-9-


The study titled “Protandim® attenuates intimal hyperplasia in human saphenous veins cultured ex vivo via a catalase-dependent pathway” was conducted by researchers at The Ohio State University and published in the journalFree Radical Biology and Medicine, vol. 50: 700-9 (2011). This study modeled the conditions that cause graft failure due to intimal hyperplasia when saphenous veins are used in surgeries to bypass blocked coronary arteries. Treatment with Protandim® significantly increased antioxidant enzyme activity in veins cultured at high oxygen, while reducing free radical levels, lipid peroxidation, and, importantly, reducing intimal proliferation to the level seen in normal healthy saphenous vein.

The researchers at Louisiana State University have authored a review paper titled “The role of manganese superoxide dismutase in skin cancer” in the journalEnzyme Research, vol. 2011, Article ID 409295 (2011). This paper reviews their findings with Protandim® (as described above) in the context of published research by others in the field.

A company-sponsored study titled “Oxidative stress in health and disease: the therapeutic potential of Nrf2 activation” was published in the journalMolecular Aspects of Medicine, Aug;32(4-6):234-46 (2011). This study compared in vitro the Nrf2-activating ability of Protandim® to those of the pharmaceutical Nrf2 activators bardoxolone methyl and BG12. It also analyzed the gene expression profile induced by Protandim vis-à-vis those produced by atherosclerosis, colon cancer, and Alzheimer’s disease.

Results of a human clinical trial of Protandim® in withdrawing alcoholics were published in theAmerican Journal of Physiology: Lung Cell Mol Physiol. Apr;302(7):L688-99 (2012). The subjects, whether treated or untreated, failed to show the anticipated detrimental changes inalveolar epithelial permeability or intrapulmonary oxidative stress thought to accompany alcohol withdrawal, precluding any observations of efficacy. The study did, however, provide an additional study of safety in humans at an elevated dosage of Protandim®. No adverse events were observed.

Researchers at Colorado State University have authored a paper titled “Phytochemical activation of Nrf2 protects human coronary artery endothelial cells against an oxidative challenge” in the journalOxidative Medicine and CellularCell Longevity, 2012:132931 (2012). This paper reports their findings that ProtandimExercise & Sports Science Reviews, Clinical Pharmacology, and The FASEB Journal.

LifeVantage TrueScience® causes nuclear translocation of Nrf2 in the cells that
We sell a full line human coronary arteries, providing substantial protection when these cells were exposed to oxidative stressin vitro.

LifeVantage TrueScience®

LifeVantage TrueScience® is our scientifically-basedof anti-aging skin care product which includes natural and effective ingredients. This product was formulated to protect the skin from a variety of factors that contribute to aging and the symptoms of unhealthy skin. This proprietary skin care formula was clinically tested by Kimberly Stone, M.D., a Denver-based board certified dermatologist.

Ourproducts under our LifeVantage TrueScience® product contains a number of ingredients including some of the same ingredients found in our Protandim® brand, which consists of: product. LifeVantage TrueScience® has been formulated to

improve skin tone and even skin coloring, diminish

TrueScience® Ultra Gentle Facial Cleanser: a concentrated, ultra-rich cleanser used to remove impurities and light make-up without drying or stripping natural oils in the skin.
TrueScience® Perfecting Lotion: a hybrid lotion formulated for smoother, radiant and brighter looking skin.
TrueScience® Eye Corrector Serum: a serum that noticeably improves the visible signs of fine lines, creases and wrinkles around the entire eye area, diminishes puffiness above and below the eye, and evens skin tone and dark circles that are visible signs of premature aging.
TrueScience® Anti-Aging Cream: a cream that deeply moisturizes and helps to combat the appearance of fine lines and wrinkles, and provide a vibrant, healthy and glowing appearance. LifeVantage TrueScience® is also designed to improve skin smoothness and pigmentation, while increasing skin moisture.

The LifeVantage TrueScience® formula offers:

Hydration/Moisturizing:LifeVantage TrueScience® features a Lamellar Phase Emulsion System that forms a liquid emulsion barrier for superior moisturizing. This is accomplished by delivering exotic fatty acids to retain the body’s natural moisture and produce a moisturizing effect. It also features sodium hyaluronate, a superior moisture-binding agent that can balance moisture levels at the surface of the skin.

-10-


Toning/Brightening:The turmeric extract in LifeVantage TrueScience® is specially modified to remove yellow compounds in the skin without reducing the effectiveness of its potent curcuminoids. Curcuminoids have been shown to produce skin lightening that evens dispigmentation. Additionally, the ingredient leucojum aestivum bulb extract is believed to slow the spread of pigment-producing cells that contribute to uneven skin coloring.

Minimizing Wrinkles/Fine Lines:The palm peptides and leucojum aestivum bulb extract in LifeVantage TrueScience® have been shown to visibly reduce signs of wrinkles and fine lines and to promote improved skin tone and texture.wrinkles.

Lipid Rejuvenation:LifeVantage TrueScience® delivers multiple ingredients intended to mimic the naturally occurring lipid structure in the skin and retain the body’s own moisturizing lipids.

These products were tested in an independent third-party clinical study and were shown to reduce the visible signs of aging by utilizing Nrf2 technology to mitigate the visible effects of skin damage caused by oxidative stress. Our LifeVantage TrueScience® skin care products leverage our research on Nrf2 activation and oxidative stress.

- 7-



Canine Health®
Canine Health® is a supplement specially formulated to combat oxidative stress in dogs through Nrf2 activation. Canine Health® builds upon the active ingredients in Protandim® to reduce oxidative stress, and support joint function, mobility and flexibility in dogs. Canine Health® received the Quality Seal from the National Animal Supplement Council.
Axio®
We introduced our energy drink, Axio®, in October 2014. Axio® is formulated to promote alertness and support mental performance. LifeVantage energy drink powders deliver sustained energy, as well as improved mental focus and promote a positive mood. Axio® is derived from a unique combination of scientifically validated ingredients.
Distribution of Products

We believe our products are well-suitedwell suited for person-to-person sales through a network marketing distribution system for several reasons:

Ourour direct selling model. This model allows our independent distributors can provide extensive education to end userseducate our customers regarding the benefits of our unique products about the benefits and distinguishing characteristics of each product through a variety of meetings andmore thoroughly than other interactions;

business models. Our direct selling model also allows our independent distributors canto offer personalized customer service to thoseour customers and encourage regular use of our products.

Product Return Policy
All products purchased directly from us include a customer satisfaction guarantee. Subject to some exceptions based on local regulations, customers may return unopened product to us within 30 days of purchase for a refund of the purchase price less shipping and handling. In addition, our inventory repurchase program allows independent distributors who terminate their distributorship to return certain amounts of unopened, unexpired product purchased within the prior 12 months for a refund of the purchase price less a 10% restocking fee. The amount of inventory we will repurchase from an independent distributor is subject to specified consumption limitations.
Customers
We generally categorize our customers as independent distributors and preferred customers.
Independent Distributors
An independent distributor in our company is someone who participates in our network marketing business opportunity by purchasing our products at wholesale prices and selling our products to others interested in the products. We believe our independent distributors are typically entrepreneurs who believe in our products and business opportunity and encourage repeat use of our products; and

We can offer an opportunity to not only use our products, but to build an independent business that has the potential for creating long-term residual income to independent distributors.

Customers

We have attracted a large number of customers who not only want the health benefits of our products, but who also want to sell these products and develop an independent business. We also have customers who regularly purchase and consume our products for personal use only. These customers include both long-term users of our products and those who have recently been introduced by our independent distributors and want the benefit of our products, but are not interested in becoming independent distributors. As a result, we have developed a unique customer base. We define our customers in three categories:

Independent Distributors: Independent distributors are those who purchase our product on a recurring, monthly basis and build their own distribution business;

Preferred Customers: Preferred customers are those who purchase our products at our wholesale price on a monthly auto-ship basis for personal consumption, without the intent to resell; and

Retail Customers: Retail customers are those who sporadically purchase our products at our suggested retail prices.

Independent Distributors

Independent distributors are defined within the network marketing industry in various ways. Each company has its own methodology for differentiating between distributors and customers. We define an independent distributor as someone who has purchased a business pack containing product and sales aids and who intends to sell product to, and actively enroll, other independent distributors and/or preferred customers. Our plan requires the purchase of product to participate in our compensation plan. Currently independent distributors can purchase a basic or advanced starter kit. Our independent distributors are entrepreneurs who desire to earn income and

-11-


buildby building a business of their own, and who see greatown. Many of our independent distributors are attracted by the opportunity in sellingto sell unique, scientifically validatedscientifically-validated products without incurring significant start-up costs. We provide the business plan and extensive training along with the products and marketing sales aids, and independentIndependent distributors sign a contract with us that containsincludes a requirement that they adhere to strict policies and procedures for running an independent home-based business.procedures. Independent distributors have different buying habits than our other customers. They not only purchase product from us for individual consumption, but also purchase small quantities of product from us to use for demonstrations and one-off, person-to-person retailing opportunities, along with product and business sales tools that help them withopportunities. They also spend a large amount of their business.

We rely ontime encouraging others to purchase our existing independent distributors to attract and sponsor new distributors of our products. products, either for personal consumption or resale.

While we provide Internet support, product samples, brochures, magazines, and other sales and marketing materials, independent distributors are primarily responsible for attracting, enrolling and educating new independent distributors with respect to our products and compensation plan. An independent distributor creates multiple levels of compensation by selling our compensation plan,products and how to build a successful distributorship. Enrollingenrolling new independent distributors creates multiple levels in a network marketing structure. Sponsoredwho sell our products. These newly enrolled independent distributors are also referred to asform a “downline” distributors.for the independent distributor who enrolled them. If downline independent distributors also sponsorenroll new independent distributors who purchase our products, they create additional levels in the network marketing structure, butof compensation and their downline independent distributors remain in the same downline network as theirthe original sponsoringenrolling independent distributor. Sponsoring activities are not requiredWe pay commissions only upon the sale of distributors and weour products. We do not pay any commissions for sponsoring newenrolling independent distributors, unless the new independent distributors also purchase products. However, because of the financial incentives provided to those who succeed in building and mentoring a distributor network that resells and consumes products, many of our independent distributors do sponsor additional distributors.

We define “active independent distributors” under our compensation plan as those independent distributors who have purchased product from us for retail or personal consumption during the prior three months. As of June 30, 20122015, we had approximately 46,00065,000 active independent distributors compared to approximately 16,00068,000 active independent distributors as of June 30, 2011.

Despite the positive increases that we have experienced in our first three years with our network of independent distributors, these numbers can fluctuate from year to year based on several factors, including the opening of new geographic markets, changes in leadership, product life cycles and general economic conditions. We may also experience seasonal fluctuations in independent distributor enrollment because of holidays and vacation periods. We cannot predict the timing or degree of fluctuations because of the multiple factors that impact distributors and home based businesses. We cannot assure you that the number, growth or productivity of our independent distributors will be sustained at current levels or increase in the future.

2014Preferred Customers.

We have a substantial base of preferred customers, which we consider to be one of our competitive advantages. We define preferred customers as those customers who purchase our products at our wholesale price on a monthly auto-ship basis for personal consumption, without the intent to resell. A preferred customer may enroll as an independent distributor at any time, should they decide they are interested in reselling the product or participating in our compensation plan.

Independent Distributor Compensation
We believe our preferred customers are a great sourcecompensation plan is one of word-of-mouth advertising for LifeVantage and our products. We also believe our large base of preferred customers provides credibility to our company by validating the attractiveness of our products, separate from the network marketing business opportunity.

We engage in regular marketing activities targeted to retaining our preferred customers. These marketing activities are conducted both through our independent distributors’ personal contacts and product information included in product orders. We define an “active preferred customer” as a preferred customer who has purchased product from us within the prior three months.

-12-


As of June 30, 2012 we had approximately 119,000 active preferred customers compared to approximately 35,000 active preferred customers as of June 30, 2011.

Retail Customers

Our retail customers purchase product for individual consumption on a one-time or sporadic basis at the suggested retail price and add to the validation of our products as desirable to a broad customer base. Retail customers do not sponsor new independent distributors, sign up new customers, participate in our recurring auto-ship program or in our compensation plan. They do, however, receive the unique benefits of our products, as well as product information in their orders.

Independent distributors can also resell our products directly to retail customers. These secondary sales of products from our independent distributors to retail customers are not included in our sales numbers.

Independent Distributor Compensation

We build and maintain our distributor network by offeringmore financially rewarding and flexible career opportunitiesin the direct selling industry. Our percentage of sales paid to independent distributors to sell high quality, science-backed, innovativeas compensation and efficacious products to consumers seeking a healthy lifestyle. We believeincentives is one of the income opportunity provided byhighest percentages reported in the direct selling industry. Some elements of our compensation plan appealsare paid weekly. We believe this gives us a competitive advantage and helps retain new distributors by allowing them to experience success quickly from their efforts. Our compensation plan is intended to appeal to a broad cross-section of people, particularly those seeking to supplement family income, start a home-basedhome-


- 8-



based business or pursue entrepreneurial opportunities full or part-time. Our independent distributors earn compensation by selling our productson their product sales and can also earn commissions and bonuses on product sales made by otherindependent distributors who joinwithin their sales organizations.

Independent distributors earn compensation primarily in two ways:

from commissions on products that are purchased by distributors and customers within their individual organizations; and

through retail markups on sales of products purchased by theorganization, or "downline." Our independent distributors can also earn money by purchasing product from us at our wholesale cost.

Independent distributors are thus incentivized to sellcost and selling that product to and sponsor other independent distributors and establish their own sales organizations. Each independent distributor’s success is dependent on two primary factors:

others at the time, effort and commitment put into his or her business; and

the product sales made by him or her and his or her sales organization.

retail cost. We offer our independent distributors a competitive sales compensation plan. Under our compensation plan, an independent distributor is paid monthly and sometimes weeklygenerally pay commissions in the distributor’s home country, in local currency (based on U.S. dollars), forof the independent distributor’s own product sales and for product sales in that independent distributor’s downline network across all geographic markets. We believe our distributor compensation plan, along with the opportunity for international expansion and increased programs for distributor recognition, will continue to motivate and compensate our independent distributors to increase sales of our products.

home country.

Independent Distributor Motivation and Training

We believe that motivation

Our revenue depends in part on the success and training are essential elements in the successproductivity of our independent distributorsdistributors. Our Master Track program is designed to increase our independent distributors' productivity and we have established a broad array of motivational, educational and support services to support these needs. These services include:

increase their potential for success. The Master Track program includes the following components:

providing

Blueprint for Prosperity: professionally-designed training materials independent distributors can utilize in their sales and recruiting efforts;

-13-


a motivating, performance-based compensation plan;

individual recognition, reward programs and promotions; and

participation in local, national and worldwide company-sponsored sales events.

During the past fiscal year, we andPro Audio Series: our weekly audio series presented by our independent distributors conducted thousands ofdistributor leaders providing training sessionsand tips on becoming more productive independent distributors;

Premier Schools: monthly, company-sponsored events held throughout the U.S., and less frequently in Japan, designed to educatedeliver training and motivation to independent distributors;
Elite Academy and Global Convention: quarterly and annual company-sponsored events intended to provide training and motivation to our independent distributors; and
Promotions and Incentive Trips: we hold special promotions and incentive trips from time to time in order to motivate our independent distributors on how to develop business-building and leadership skills and how to differentiate our products to consumers. accomplish specific sales goals.
In addition to the Master Track program, we sponsor our onlinehave an on-line media channel, LVN Media, channel,through which deliverswe deliver educational and motivational and inspirational content from our executive officers and independent distributor leaders. We also have our corporate-sponsored training events that provide a forum for distributors, who otherwise operate independently, to share ideas with us and with each other.

We also enable our independent distributors to succeed through our ongoing efforts to secure coverage of our sciencedistributors. The Master Track program and products by various media outlets. We have received media and editorial coverage from, among others, Dr. Phil, ABC’s “Primetime,” NBC’s “Today,” PBS’s “Healing Quest,” “Vitamin Retailer” magazine, “Rodeo News,” “5280” magazine, “The Direct Selling News,” “Delicious Living” magazine, “Utah Women” magazine, “CEO/CFO” online magazine, “Utah Valley BusinessQ” magazine and the — “AARP Magazine”. We have also had media appearances from our company spokesperson, Donny Osmond, including references of Protandim in “Living Well” magazine and on “Entertainment Tonight.”

Distributor Compliance Activities

We monitor independent distributor activity in each market as partLVN Media are important parts of our efforts to enforceincrease the productivity and potential for success of our policiesindependent distributors. We are evaluating how to incorporate new technology and procedures. These policies and procedurestraining opportunities to improve distributor success.

Distributor Compliance Activities
Given that our independent distributors are independent contractors, we do not control or direct their promotional efforts. We do, however, require that our independent distributors comply with federal, state and local laws. Theabide by policies and procedures also establish other rules that our independent distributors must follow. We require our independent distributorsthem to present products and business opportunities ethically, professionallyact in an ethical manner and in compliance with applicable laws and regulations. Independent distributors further agree that their presentations to customers must be consistent with,As a member of the United States Direct Selling Association and limitedsimilar organizations in many of the markets where we do business, we are also subject to the product claimsethical business practices and representations made in our literature for each country.

consumer service standards required by the industry's code of ethics.

Independent distributors must represent to us that their receipt of commissions is based on retail sales and substantial personal sales efforts. We must produce or pre-approve all sales aids used by distributors such as brochures and online materials. Products may be promoted only by personal contact or by collateral materials produced or approved by us. Independent distributors may not use our trademarks or other intellectual property without our consent.

We monitor and systematically review alleged independent distributor misbehavior through our internal compliance department. If we determine one of our independent distributors has violated any of our policies orand procedures, we may discipline the independent distributor and may terminate the independent distributor’s rights to distribute our products. When necessary, we have brought legal action against independent distributors, or former independent distributors, to enforce our policies and procedures. Short of termination or legal action, we may impose sanctions such asagainst independent distributors whose actions are in violation of our policies and procedures. Such sanctions may include warnings, probation, withdrawal or denial of an award, suspension of privileges of a distributorship, fines and/or withholding of commissions until specified conditions are satisfied, or other appropriate injunctive relief.

Preferred Customers
Preferred customers are customers who purchase products directly from us at our wholesale price on a monthly auto-ship basis for personal consumption, without the intent to resell or earn commissions from the sale of products. A preferred customer may enroll as an independent distributor at any time if he or she becomes interested in reselling the product. We believe our preferred customers are a great source of word-of-mouth advertising for our products. We also believe our large base of preferred customers validates the benefits of our products, separate from the direct selling business opportunity.

- 9-



We define an “active preferred customer” as a preferred customer who has purchased product from us within the prior three months. As of June 30, 2015, we had approximately 115,000 active preferred customers compared to approximately 128,000 active preferred customers as of June 30, 2014.
Sales of ourOur Products

We accept orders for our products through our own website at www.lifevantage.com and through personalized websites we provide to our independent distributor websites,distributors, which we refer to as “Virtual Offices”, that we provide to our independent distributors as part of our network marketing program. We also accept orders for our products through our website at www.lifevantage.com.. Orders placed through Virtual Offices and through our website are processed daily at our fulfillment center,centers, where orders are shipped directly to the consumer.

We offer a toll-free number tonumbers for our independent distributors and other customers to order product or ask questions. Our customer service representatives answer customer calls and placeassist customers in placing orders inthrough our web order processing system, as well as answer questions, track packages, and provideinitiate refunds. The customer service representatives receive

-14-


extensive training and are particularly knowledgeable about our products and adept at “up-selling” customers to our auto-ship purchasing option, which allows us to realize recurring revenue on a monthly basis with no further action required by the customer.direct selling business model. Independent distributors and preferred customers generally pay for products by credit card, prior to shipment, and as a result, we carry minimal accounts receivable.

Seasonality
In addition to general economic factors, we are impacted by seasonal factors and trends such as major cultural events and vacation patterns. We believe that direct selling in Japan and the United States is also generally negatively impacted during our first fiscal quarter, from July 1 through September 30, when many individuals, including our independent distributors, traditionally take vacations.
Although our product launch process may vary by market, we may introduce new products to our independent distributors and customers through limited-time offers and promotions. The limited-time offers and promotions typically generate significant activity and a high level of purchasing, which may result in a higher than normal increase in revenue during the quarter of the limited-time offer and skew year-over-year and sequential comparisons.
Geographic Information
We currently sell and distribute products in the United States, Japan, Hong Kong, Australia, Canada, Philippines, Mexico and Thailand. In fiscal year 2015, revenue generated in the United States accounted for approximately 70% of our total revenue and revenue generated from Japan accounted for approximately 22% of our total revenue. For reporting purposes, we generally divide our markets into two geographic regions: Americas and Asia/Pacific. The following table sets forth net revenue information by region for the periods indicated (in thousands):
 For the years ended June 30,
 2015 2014 2013
Americas$138,118
 72.6% $141,227
 66.0% $133,046
 63.9%
Asia/Pacific52,218
 27.4% 72,741
 34.0% 75,132
 36.1%
Total$190,336
 100% $213,968
 100% $208,178
 100%
Additional comparative revenue and related financial information is presented in the section captioned "Segment Information" in Note 2 to our Consolidated Financial Statements.
Marketing

We have a sales, marketing, public relations and customer service group consisting of 81166 full-time employees as of June 30, 2012.2015. We utilize our network of independent distributors located throughout the United States, Australia, Hong Kong, Japan, Canada, Philippines, Mexico Australia and JapanThailand to market and sell our products.

Raw Materials and Manufacturing

We outsource the primary manufacturing, fulfillment, and shipping components of our business to companies we believe possess a high degree of expertise. Outsourcing allowsWe believe outsourcing provides us to avoid the relatively high fixed costs of hiring manufacturing personnel and building our own infrastructure to accomplish these same tasks, while gaining access to advanced manufacturing process capabilities and expertise.

expertise without incurring fixed costs associated with manufacturing our own products.

In July 2008, we entered into aWe currently outsource the manufacturing of Protandim® to multiple contract manufacturing agreement with Cornerstone Research & Development, Inc., or Cornerstone, under which Cornerstone manufacturesmanufacturers and packages Protandim. Our sales growth in fiscal year 2011 led us to secure a second manufacturer, Deseret Laboratories International, or Deseret. This secondary manufacturer significantly reduces our dependence onuse a single contract manufacturer for Protandimeach of our Canine Health®., Axio

Cornerstone ®and Deseret, as theLifeVantage TrueScience® products. Our contract manufacturers of Protandim®, have a legal obligation to comply with the Currentcurrent Good Manufacturing Practices regulations that are applicable to those who manufacture, package, label and hold dietary supplements. Additionally, we are subject to regulations that, among other things, obligate us to know what and how manufacturing activities are performed so that we can make decisions related to


- 10-



whether the packaged and labeled product conforms to our established specifications and whether to approve and release product for distribution. We maintain and qualify otheralternative manufacturing options in order to keep our costs low, maintain the quality of our products, and to be prepared for unanticipated spikes in demand or manufacturing failure. Cornerstone and DeseretOur contract manufacturers deliver products to our fulfillment centercenters based on our purchase orders.
We acquire raw materials for our products from third-party suppliers. Although we generally have good relationships with our suppliers, we believe we could replace any of our current suppliers without great difficulty or significant increase to our cost of goods sold. We also have ongoing relationships with secondary and tertiary suppliers. Please refer to "

Risk Factors - High quality material for our products may be difficult to obtain or expensive" for a discussion of the risks and uncertainties associated with our sourcing of raw materials.

Product Liability and Other Insurance
We have product liability insurance coverage for our products that we believe is adequate for our needs. We also outsourced the manufacturing of LifeVantage TrueSciencemaintain commercial property and liability coverage and directors’ and officers’ liability insurance.
Intellectual Property
Protandim® is a proprietary, patented dietary supplement formulation for enhancing antioxidant enzymes including superoxide dismutase and catalase. The patents and patent applications protecting this formulation are held by our wholly-owned subsidiary, Lifeline Nutraceuticals Corporation.
We use commercially reasonable efforts to Wasatch Product Development, LLC, or Wasatch. Wasatch’s core competencyprotect our intellectual property and license rights through patent protection, trade secrets, and contractual protections, and intend to continue to develop a strong brand identity in the Protandim® trademark.
Our intellectual property is sourcingcovered, in part, by six issued U.S. patents and manufacturing cosmeticsfive issued foreign patents in Australia, Canada, China, Japan and India. A corresponding foreign patent application is pending in Europe. Our patents and patent applications claim the benefit of priority of seven U.S. provisional patent applications, the earliest of which was filed on March 23, 2004, and relate to compositions, methods of use, and methods of manufacture of various compositions, including those embodied by the Protandim® formulation. The expected duration of our patent protection via granted patents is through approximately March 2025.
We also continue to protect our products and brands using trademarks. We have filed and successfully procured registered trademarks for both U.S.Protandim®, LifeVantage®, and international customers.TrueScience

COMPETITION®

Network Marketing in many countries around the world, and we have pending trademark applications in many other countries. We anticipate seeking protection in other countries as we deem appropriate.

In order to protect the confidentiality of our intellectual property, including trade secrets, know-how and other proprietary technical and business information, it is our policy to limit access to such information to those who require access in order to perform their functions and to enter into agreements with employees, consultants and vendors to contractually protect such information.
Competition
Direct Selling Companies

We compete with other direct selling companies, that sell their products through network marketing, many of which have a longer operating historyhistories and greater visibility, name recognition and financial resources than we do. We also compete with newer direct selling companies that attempt to solicit our independent distributors by offering the possibility of a more financially rewarding opportunity by being among the company's early distributor base. We compete for new independent distributors with these companies on the strengthbasis of our business opportunities,opportunity, product offerings, compensation plan, management and our operations. In order to successfully compete in the network marketingdirect selling industry and attract and retain independent distributors, we must maintain the attractiveness of our business opportunity, product offerings and products.

compensation plan.

Dietary Supplement Market

We compete with other companies inthat sell dietary supplements. We believe the dietary supplementssupplement market which is a highly fragmented and competitive market. We believe competition in the dietary supplement market is based primarily on quality, price, efficacy of products, brand name and brand name.recognition of product benefits. In the dietary supplement industry, our competition includes numerous nutritional supplement companies, pharmaceutical companies and packaged food and beverage companies. Many of these companies have broader product lines, and larger sales volumes than us and have

-15-


greater financial and other resources available to them.than we do. Additionally, some of these companies are able to compete more effectively due to greater vertical integration. Increased


- 11-



competition in the dietary supplement market could have a material adverse effect on our results of operations and financial condition.

Nrf2 Activators

Protandim® is one of a few products designed and marketed to activate the transcription factor Nrf2.

In the dietary supplement market,last few years we have seen the number of products marketed as Nrf2 activators increase, and we are currently aware of at least two other dietary supplementfive such products. We anticipate the number of products that claim to activate Nrf2 activation, like Protandim®.

will continue to increase as the technology becomes more popular and more broadly accepted. Although we are unaware of any competing direct selling company marketing products as Nrf2 activators, we are aware that at least two competing direct selling companies have sponsored research studies related to Nrf2 activation.

Direct Antioxidants

Vitamin C, Vitamin E, Coenzyme Q-10, and other sources of externally derived antioxidants may be considered competitors of Protandim® but they are mechanistically distinct from Protandim®. These other sources of antioxidants do not increase the body’s elimination of oxidants using internal antioxidant enzymes. Our research indicates that Protandim® increases production of hundreds of stress-related anti-inflammatory, and anti-fibrotic gene products including antioxidant enzymes, such as superoxide dismutase and catalase, within the cells of the body. We believe that the body’s internally produced antioxidant enzymes provide a better defense against oxidative stress than externally derived sources of antioxidants.

Oral Superoxide Dismutase and Catalase

There are many companies performing research into antioxidants, and these companies are intensely competitive.antioxidants. Several companies sell oral forms of superoxide dismutase and catalase. Although we believe Protandim® is a superior alternative to oral forms of superoxide dismutase and catalase, which make claims thatthese products do compete with Protandim®. However, due to research which indicates in the lack of bioavailability and efficacy of such oral delivery, we believe Protandim® to be a superior alternative. One or moremarketplace. We anticipate additional companies maywill likely develop, purchase or license from a third party,in-license products which may bethat are competitive with Protandim®.

Personal Skin Care Market

In the personal skin care market, we compete principally with large, well-known cosmetics companies that manufacture and sell broad product lines through various types of retail establishments. Many of these competitors have significant competitive advantages over us due to their greater financial resources and brand recognition. However,recognition than we do. We believe, however, we can compete with these larger companies due toby leveraging our direct selling model and emphasizing our unique, scientifically basedscience-based skin care product.

REGULATORY ENVIRONMENT

Product Liabilityproducts.

Animal Supplement Market
We compete principally with large, well-known companies in the animal supplement market. Most of the companies we compete with in the animal supplement market have broad distribution channels that include retail establishment. Many of these competitors have greater financial resources and Other Insurance

brand recognition than we do. We believe, however, we can compete with these larger companies by leveraging our direct selling model and emphasizing our unique, science-based animal supplement product.

Energy Drink Market
We compete with large, well-known companies in the energy drink market. Most of the companies we compete with in the energy drink market have product liability insurance coverage forbroad distribution channels that include big box retail establishments. Many of these competitors have greater financial resources and brand recognition than we do. We intend to compete with these larger companies by leveraging our products that we believe is adequate fordirect selling model and emphasizing our needs. We have also obtained commercial property and liability coverage, as well as directors’ and officers’ liability insurance.

Intellectual Property

Protandim®unique, science-based energy drink product. Axio is a proprietary, patented dietary supplement formulation for enhancing antioxidant enzymes including superoxide dismutaseno sugar, low-carbohydrate and catalase. The patentslow calorie energy drink that is also non-GMO, gluten-free and patent applications protecting this formulation are held by our wholly-owned subsidiary, Lifeline Nutraceuticals Corporation.

We use commercially reasonable efforts to protect our intellectual property and license rights through patent protection, trade secrets, and contractual protections, and intend to continue to develop a strong brand identity in the Protandim® trademark.

-16-


Our intellectual property is covered, in part, by five U.S. patents issued in July 2007, June 2008, August 2009, April 2011, and July 2012. One U.S. Utility Patent application is currently pending in the U.S. Patent and Trademark Office and additional filings are anticipated. Corresponding patents directed to the Protandim® formulation have now also been granted in Australia, China, and India and applications are currently pending in Canada, Europe, and Japan. Our patents and patent applications claim the benefit of priority of seven U.S. provisional patent applications, the earliest of which was filed on March 23, 2004, and relate to compositions, methods, and methods of manufacture of various compositions, including those embodied by the Protandim® formulation. The expected duration of our patent protection via granted patents is through March 23, 2025.

Protandim® is a registered trademark in the United States, Australia, Canada, China, Costa Rica, the European Community, Japan, Mexico, New Zealand and Taiwan.

We have applied for registration of the trademark LifeVantage™ through the World Intellectual Property Organization, or WIPO. We have registered the mark LifeVantage® in the United States, Canada and Mexico and through WIPO in Australia, China, Japan, New Zealand and the European Community. The LifeVantage TrueScience® mark is registered in the United States, the European Community, Australia, New Zealand, Mexico, Japan, Norway, Singapore, Switzerland and the Russian Federation.

In order to protect the confidentiality of our intellectual property, including trade secrets and know-how and other proprietary technical and business information, it is our policy to limit access to such information to those who require access in order to perform their functions and to enter into agreements with employees, consultants and vendors to contractually protect such information.

Governmental Regulations

FDA Regulations

vegan.

Regulatory Environment
The formulation, manufacturing, packaging, labeling, and advertising of our Protandim® and LifeVantage TrueScience® products in the United States are subject to regulation by the Food and Drug Administration, or FDA, and the Federal Trade Commission, or FTC, as well as comparable state laws. We are not required to obtain
FDA pre-market approval to sell our Protandim® supplement in the United States.

Regulations and DSHEA

We market Protandim® as a “dietary supplement” as defined in the Dietary Supplement Health and Education Act of 1994, or DSHEA. DSHEA is intended to promote access to safe, quality dietary supplements, and information about dietary supplements. DSHEA established a new framework governing the composition and labeling of dietary supplements. DSHEA does not apply to animal supplements like Canine Health

®. We are not required to obtain FDA pre-market approval to sell our products in the United States under current laws.


- 12-



DSHEA permits statements of nutritional support, called “structure-function” statements, to be included in labeling for dietary supplements without FDA marketing approval. Such statements may claim a benefit related to a classical nutrient deficiency disease and disclose the prevalence of such disease in the United States, describe the role of a nutrient or dietary ingredient intended to affect the structure or function in humans, characterize the documented mechanism by which a nutrient or dietary ingredient acts to maintain such structure or function, or describesdescribe general well-being from consumption of a nutrient or dietary ingredient. Such statements may not expressly or impliedly claim that a dietary supplement is intended to diagnose, cure, mitigate, treat, or prevent a disease. A company that uses a statement of nutritional support in labeling must possess evidence substantiating that the statement is truthful and not misleading and is supported by competent and reliable scientific evidence.
The FDA may assert that a particular statement of nutritional support that a company is using is an illegal claim; that assertion, normally, is in the form of a warning letter to that company. We have a duty to send to the FDA a notice that lists each new structure-function statement made by us; we are obligated to send that notice within 30 days after the first marketing of a supplement with such a statement.

DSHEA also permits certain scientific literature, for example a reprint of a peer-reviewed scientific publication, to be used in connection with the sale of a dietary supplement to consumers without the literature

-17-


being subject to regulation as labeling. However, such literature must not be false or misleading, the literature may not promote a particular manufacturer or brand of dietary supplement and it must include a balanced view of the available scientific information on the subject matter, among other requirements.

The FDA, on July 5, 2011, published a draft guidance thatFDA's Center for Veterinary Medicine, or CVM, is entitled “Dietary Supplements: New Dietary Ingredient Notifications and Related Issues.” The FDA announced in June 2012, after encountering substantial criticism of some sectionsresponsible for enforcing the portion of the draft guidance,Federal Food, Drug, and Cosmetic Act, or the Act, that it intendsrelates to issue a revised NDI guidance document. The FDA has not indicated when it will do so, but it is unlikely that it will do so before November 1, 2012. Although only a draft document, the revised draft guidance will reflect the FDA’s then views on the topic of New Dietary Ingredients. The draft guidance did not affect Protandimanimal supplements, like our Canine Health® product. CVM's primary responsibility in enforcing the Act is to ensure that animal supplements are safe, effective, and we do not anticipate that the revised draft guidance will affect Protandim®, but it willcan be relevantmanufactured to other dietary supplement products and may affect us if we decide to formulate and sell dietary supplements other than Protandim®a consistent standard..

While we exercise care in our formulation, manufacturing, packaging, labeling, and advertising of Protandim®,our products, we cannot guarantee that the FDA will never inform us that the FDA believes some violation of law has occurred.occurred either by us or by our independent distributors. Any allegations of our non-compliance may result in time-consuming and expensive defense of our activities. The FDA’s normal course of action is to issue a warning letter if it believes that a product is misbranded or adulterated. The responsive action requested by the FDA differs depending upon the nature of the product and claims in question. Typically, the FDA expects a written response within fifteen15 working days of the receipt of a warning letter. The warning letter is public information posted on the FDA’s web site. That information could affect our relationships with our investors, independent distributors, vendors, and consumers. Warning letters also often spark private class action litigation under state consumer protection statutes. The FDA could also order compliance activities, such as an inspection of our facilities and products, and could file a civil lawsuit in which an arrest warrant (seizure) could be issued as to some or all of the Company’sour products. In extraordinary cases, the Company and one or more of its principalswe could be named defendantsa defendant and sued for declaratory and injunctive relief.

FTC Regulations

Advertising and marketing of our products in the United States are also subject to regulation by the FTC under the Federal Trade Commission Act, or FTC Act. Among other things, the FTC Act prohibits unfair methods of competition and unfair false or deceptive acts or practices in or affecting commerce. The FTC Act also makes it illegal to disseminate or cause to be disseminated any false advertisement. The FTC Act provides that disseminating any false advertisement pertaining to foods, which would include dietary supplements, is an unfair or deceptive act or practice. An advertiser is required to have competent and reliable scientific evidence for all express and implied health-related product claims at the time the claims are first made. We are required to have adequate scientific substantiation for all material advertising claims made for our products in the United States. The FTC routinely reviews websites to identify questionable advertising claims and practices. Competitors sometimes inform the FTC when they believe other competitors are violating the FTC Act and consumers also notify the FTC of what they believe may be wrongful advertising. The FTC may initiate a non-public investigation that focuses on our advertising claims which usually involves non-public pre-lawsuit extensive formal discovery. Such an investigation may be very expensive to defend, be lengthy, and result in a publicly disclosed Consent Decree, which is a settlement agreement. If no settlement can be reached, the FTC may start an administrative proceeding or a federal court lawsuit against us or our principal officers. The FTC often seeks to recover from the defendants, whether in a Consent Decree or a proceeding, any or all of the following: (i) consumer redress in the form of monetary relief or disgorgement of profits; (ii) significant reporting requirements for several years; and (iii) injunctive relief. In addition, most, if not all, states have statutes prohibiting deceptive and unfair acts and practices. The requirements under these state statutes are similar to those of the FTC Act.

The National Advertising Division, or NAD, of the national BBB,Better Business Bureau, a non-governmental not-for-profit organization through its Electronic Retailing Self-Regulation Program,Advertising Self-Regulatory Council, or ERSP,ASRC, is also actively engaged in conducting investigations, called “inquiries”,inquiries, which are focused on determining whether the requisite FTC claim substantiation standard exists for specific

- 13-



structure-function claims. Although the results of each inquiry or

-18-


proceeding are not binding on the recipient, they are posted on NAD’s website. We have been the subject of such a proceeding in 2008 and 2009, which was concluded in 2009. We believe it is unlikely that we will be the subject

Regulation of another such proceeding in the reasonably foreseeable future unless our national advertising claims become materially different from those that were the subject of that proceeding.

Additionally, any telemarketing activities we may engage in in the United States must comply with federal telemarketing statutes that are enforced by the FTC and state Attorneys General, and with additional telemarketing statutes and regulations of the various states. Because it may be difficult to ensure compliance with these laws and regulations by the individuals who actually make and receive such calls, there is a risk that we could be the subject of investigation and other enforcement activities that may be brought by the FTC and state agencies. We regularly train and educate our representatives and independent distributors to represent our product correctly and appropriately.

“Pyramid Scheme” Regulations

Network marketingDirect Selling Activities

Direct selling activities are regulated by the FTC, as well as various federal, state and local governmental agencies in the United States and foreign countries. These laws and regulations are generally intended to prevent fraudulent or deceptive schemes, often referred to as “pyramid” schemes, which compensate participants primarily for recruiting additional participants irrespective ofwithout significant emphasis on product sales, use high-pressure recruiting methods and/or do not involve legitimate products.sales. The laws and regulations often:

impose cancellation/product return, inventory buy-backs and cooling-off rights for consumers and distributors;

require us or our distributors to register with governmental agencies;

impose caps on the amount of commission we can pay;

impose reporting requirements; and

impose upon us requirements, such as requiringrequire that we ensure, among other things, that our distributors to maintain levels of retailproduct sales to qualify to receive commissions to ensureand that our distributors are being compensated primarily for sales of products and not primarily for recruiting new distributors.

additional participants.

The laws and regulations governing network marketingdirect selling are modified from time to time, and, like other network marketingdirect selling companies, we may be subject from time to time to government investigations related to our network marketingdirect selling activities. This may require us to make changes to our business model and our compensation plan.

State Regulations

In addition to U.S. federal regulation, each state has enacted its own food and drug laws. We may receive requests to supply information regarding our sales or advertising to state regulatory agencies. We remain subject to the risk that, in one or more of our present or future markets, our products, sales, and advertising could be found non-compliant with state laws and regulations. If we fail to comply with these laws and regulations, it could have a material adverse effect on our business in a particular market or in general. In addition, these laws and regulations could affect our ability to enter new markets.

The Bioterrorism Act

The Public Health Security and Bioterrorism Preparedness and Response Act of 2002, or Bioterrorism Act, contains requirements with regard to the sale and importation of food products in the United States, including:

mandatory registration with the FDA of all food manufacturers;

prior notice to regulators of inbound food shipments;

recordkeeping requirements, and grant of access to the FDA of applicable records; and

grant of detention authority to the FDA of food products in certain circumstances.

-19-


Under the record keeping requirements, we are considered to be a “nontransporter” of Protandim® and must maintain certain records required of nontransporters. We are in the process of ensuring that we keep all appropriate records required by the Bioterrorism Act.

The FDA Food Safety Modernization Act

The FDA Food Safety Modernization Act, or FSMA, was enacted in 2011 and is now part of the Federal Food, Drug and Cosmetic Act, or FFDCA. The FSMA is a comprehensive set of laws that gives the FDA considerable new authority with respect to the prevention of food contamination and the serious problems associated with such contamination. Among other things, it does the following:

gives the FDA explicit authority to inspect and copy allcertain records related to any food and to compel a recall if the FDA believes there is a reasonable probability of serious adverse health consequences or death;

places strict new obligations on food and dietary supplement importers to verify that food from foreign suppliers is not adulterated or misbranded; and

provides whistle blower protection for employees of conventional food or dietary supplement companies who provide information to governmental authorities about violations of the FFDCA.

International Regulations

In addition to the regulations applicable to our activities in the United States, all other markets in which we operate our business regulate our products under a variety of regulatory schemes. We typically market Protandim® in international markets as foods or health foods under applicable regulatory regimes. However, because of varied regulations, some products or ingredients that are recognized as a “food” in certain markets may be treated as a “pharmaceutical” in other markets. In the event a product, or an ingredient in a product, is classified as a drug or pharmaceutical product in any market, we will generally not be able to distribute that product through our distribution channel because of pre-marketing approvalsapproval requirements and strict regulations applicable to drug and pharmaceutical products. In Japan, for example, the Ministry of Health, Labour and Welfare, or MHLW, recently made the determination thatashwagandha was determined to be inappropriate for inclusion in food products. Ashwagandha is one of the ingredients in Protandim is inappropriate for inclusion in a food product in Japan.®. While we and many other companies disagree with thisthe assessment of ashwagandha by Japanese regulatory authorities, we will beare restricted from selling a formulation of Protandim® that contains Ashwagandha intoashwagandha in Japan.

As such, we reformulated Protandim® for the Japan market to exclude ashwagandha. This reformulated Protandim® was introduced in Japan in fiscal 2013.

Similarly, our other markets outside the United States regulate advertising and product claims regarding the efficacy of our products and require adequate substantiation of claims. As such, we are unable to claim that any of our products will diagnose,

- 14-



cure, mitigate, treat or prevent diseases. For example, in Japan, Protandim® is considered a food product, which significantly limits our ability to make any claims regarding the product. If our marketing materials or distributor marketing materials make claims that exceed the scope of allowed claims for dietary supplements, these regulatory authorities could deem our products to be unapproved drugs and we could experience substantial harm.

Potential FDA and Other Regulation

We could become subject to additional laws or regulations administered by the FDA, FTC, or by other federal, state, local or localinternational regulatory authorities, to the repeal of laws or regulations that we consider favorable, such as DSHEA, or to more stringent interpretations of current laws or regulations. Because of negative publicity associated with some adulterated or misbranded supplements, including pharmaceutical drugs marketed as dietary supplements, there has been an increased movement in the United States and other markets to expand the regulation of dietary supplements, which could impose additional restrictions or requirements in the future. In general, the regulatory environment is becoming more complex with increasingly strict regulations each year.

regulations.

The Dietary Supplement and Nonprescription Drug Consumer Protection Act requires us to report to the FDA all serious adverse events and to maintain for six years records of all adverse events, whether or not serious. An adverse event is defined as any health-related event associated with the use of a dietary supplement that is

-20-


adverse. In addition, this law requires the label of each dietary supplement, including our Protandim® product, to include a domestic address or telephone number by which the company selling the product may receive a report of a serious adverse event associated with such product. The label of Protandim® complies with that statutory provision.

Legislation known as the Dietary Supplement Labeling Act was introduced in the United States in 2013. This proposed legislation purports to help consumers distinguish between dietary supplements that are safe and those that have potentially serious side-effects or drug interactions. The Dietary Supplement Labeling Act would require dietary supplement manufacturers to disclose known ingredient risks and display mandatory warnings if a product contains an ingredient that could cause potentially serious adverse events. Although it is not currently known if, or in what form, the Dietary Supplement Labeling Act will be enacted, it could create additional regulatory burdens on our business and increase our cost of goods sold.
Employees

As of June 30, 2012,2015 and June 30, 2014, we had approximately 139166 and 201 full time employees. This number doesemployees, respectively. As of June 30, 2015, 126 of our full time employees were based in the United States, 36 were based in Japan, nine were based in Thailand and three were based in Hong Kong. We do not include our independent distributors whoin our number of employees because our independent distributors are independent contractors rather thanand not employees. We outsource our manufacturing and distribution operations.

Available Information

Our principal offices are located at 98159785 S. Monroe Street, Suite 100,300, Sandy, UT 84070. Our telephone number is (801) 432-9000 and our fax number is (801) 880-0699. Our website address is www.lifevantage.com; however, information found on our website is not incorporated by reference into this report. Our web site address is included in this annual report as an inactive textual reference only.

The reports filed with the Securities and Exchange Commission, or SEC, by us and by our officers, directors, and significant shareholders are available for review on the SEC’s website at www.sec.gov. You may also read and copy materials that we file with the SEC at the SEC’s Public Reference Room at 100 F Street, NE, Washington, DC 20549. You may obtain information on the operation of the Public Reference Room by calling the SEC at 1-800-SEC-0330.

ITEM 1A — RISK FACTORS

Because of the following risks, as well as other risks affecting our financial condition and operating results, past financial performance should not be considered to be a reliable indicator of future performance, and investors should not use historical trends to anticipate results or trends in future periods. The risks described below are those we currently believe could materially affect us. The following risks are not necessarily all of the important factors that could cause our actual results of operations to differ materially from those expressed in the forward-looking statements in this report.

Risk Factors Relating to Our Company
Because our Japanese operations account for a significant part of our business, an inability to strengthen our business and properly manage distractions among our distributors in Japan could harm our business.
Approximately 22% and 29% of our revenue for fiscal year 2015 and fiscal year 2014, respectively, was generated in Japan. We began selling our products into the market in fiscal year 2010 and opened fully supported operations in Japan in fiscal year 2013. Due to our limited experience in Japan, the initiatives we have implemented, or that we may implement in the future,

- 15-



may not be successful in galvanizing and motivating our leading independent distributors and we may be unable to retain existing leading independent distributors in Japan. There has been discord among our leading independent distributors in Japan and some of these distributors have left our company to join a competing direct selling company. If we fail to properly manage any discord among our leading independent distributors in Japan, we could lose additional leaders to competing direct selling companies, which could have a significant negative impact on our revenue.
In addition, the regulatory framework in Japan has changed since we first started selling into the market. In fiscal year 2013, for example, we announced the release for the Japanese market of a new formulation of Protandim

® in response to the determination of the Ministry of Health, Labour and Welfare, or MHLW, that one of the ingredients in Protandim® is inappropriate for inclusion in a food product in Japan. Our business in Japan could be substantially harmed if this formulation of Protandim® faces additional challenges from regulatory agencies in Japan or if it does not gain the acceptance that the original formulation has obtained in other markets.

Other factors that could impact our results in Japan include:
inappropriate activities by our independent distributors and any resulting regulatory actions against us or our independent distributors;
continued or increased levels of regulatory or media scrutiny of our industry and any regulatory actions, or any adoption of more restrictive regulations, in response to such scrutiny;
significant weakening of the Japanese yen;
increased regulatory constraints with respect to the claims we can make regarding the efficacy of our products, which could limit our ability to effectively market our products;
improper practices of other direct selling companies or their independent distributors that increase regulatory or media scrutiny of our industry; and
weakness in the economy or consumer confidence.
There is a high level of regulatory scrutiny of the direct selling industry in Japan, and several direct selling companies have been penalized for actions of distributors that violated applicable regulations. Such penalties have included suspension from sponsoring activities in Japan. If our distributors fail to comply with applicable regulations in Japan, regulators could take action against us, including a suspension of our sponsoring activities, or we could receive negative media attention, either of which could harm our business significantly.
We may not be successful in expanding our operations.

Our fiscal year that ended June 30, 2009 was the first year since fiscal 2005 that we were able to achieve operating profits. Although we experienced significant growth in fiscal 2011 and 2012, we

We may not be successful in expanding our operationsoperations. Although we began to sell our products through our direct selling network in future periods. Becausefiscal year 2009, we still have limited experience selling products through network marketing, particularly outside the United States, and our experiencein selling our products through direct selling compared to other sales channels has not been sufficient to generate consistent operating profits,companies in our industry. As such, we may have limited insight into trends, disruptions and other factors that may emerge and affect our business. For example, we may need to terminate one or more of our independent distributors for actions contrary to their contractual obligations with us, which may slow our growth by causing a disruption among our independent distributors. Additionally, we may not be successful in keeping our leading independent distributors focused and motivated or in aligning their goals with the goals of our company. We may make errors in predicting and reacting to relevant business trends, which could harm our business. Wealso have limited experience in expanding into new geographic markets. We began selling into Mexico and Japan in fiscal year 2010 and in Australia in fiscal year 2012. Although we are seeking to continue our expansion, if we fail to effectively expand our operations into additional markets, we may be unable to generate consistent operating profit growth.

growth in future periods.

If we are able to expand our operations, we may be unable to successfully manage our future growth.

Since we initiated network marketing sales in fiscal 2009, ourgrowth.

Our business has grown significantly.significantly since we initiated our direct selling model in fiscal 2009. This growth has placed substantial strain on our management, operational, financial and other resources. If we are able to continue expanding our operations in the United States and in other countries where we believe our products will be successful, we may experience periods of rapid growth, which will require additional resources. Any such

-21-


growth expansion could place increased strain on our management, operational, financial and other resources, and we will need to train, motivate, and manage employees, as well as attract management, sales, finance and accounting, international, technical, and other professionals.resources. In addition, we will needan inability to expand the scope ofleverage our infrastructure and our physical resources. Any failure to expand these areas and implement appropriate procedures and controlscurrent resources in an efficient manner and at a pace consistent with our business objectives could have a material adverse effect on our business, operating margins and results of operations.

Because our Japanese operations account for a significant part of our business, an inability to strengthen our business and work with continued government regulations in Japan could harm our business.

Approximately 28% of our fiscal 2012 revenue was generated in Japan. The Japanese market has changed significantly since we began selling into the market in fiscal 2010 and its regulatory framework continues to change. In 2011, for example, the Ministry of Health, Labour and Welfare, or MHLW, made the determination that Ashwagandha, one of the ingredients in Protandim®, is inappropriate for inclusion in a food product in Japan. While we and many other companies disagree with this assessment, we will be restricted from selling into Japan a formulation of Protandim® that contains Ashwagandha. If we are unable to produce an equivalent or similar alternative formulation of Protandim, or if the market does not accept any such alternative formulation of Protandim, our business in Japan could be harmed substantially. Other factors that could impact our results in Japan include:

continued or increased levels of regulatory or media scrutiny and any regulatory actions taken by regulators, or any adoption of more restrictive regulations, in response to such scrutiny;

significant weakening of the Japanese yen;

increased regulatory constraints with respect to the claims we can make regarding the efficacy of Protandim® , which could limit our ability to effectively market that product;

the initiatives we have implemented in Japan, which are patterned after successful initiatives implemented in the U.S., may not generate renewed growth or increased productivity among our independent distributors in Japan, and may cost more or require more time to implement than we have anticipated;

inappropriate activities by our independent distributors and any resulting regulatory actions against us or our independent distributors;

improper practices of other direct selling companies or their independent distributors that increase regulatory or media scrutiny of our industry; and

any weakness in the economy or consumer confidence.

We rely on our information technology systems to manage numerous aspects of our business, and a disruption in these systems could adversely affect our business.

We depend on our information technology, or IT, systems to manage numerous aspects of our business, including our finance and accounting transactions, to manage our independent distributor compensation plan and provide analytical information to management. Our IT systems are an essential component of our business and growth strategies, and a serious disruption to our IT systems could significantly limit our ability to manage and operate our business efficiently. These systems are vulnerable to, among other things, damage and interruption from power loss or natural disasters, computer system and network failures, loss of telecommunications services, physical and electronic loss of data, security breaches and computer viruses. Any disruption could cause our business and competitive position to suffer and adversely affect our business and operating results.

-22-


We may not succeed in growing existing markets or opening new markets.

In fiscal year 2010 we launched

We have international operations in Japan, Hong Kong, Canada, Australia, Philippines, Mexico and Japan and inThailand. In fiscal year 20122015, we launched international operations in Australia. During fiscal year 2012, we derivedgenerated approximately 29%30% of our revenues from our international operations.operations, most of which was generated from Japan. We believe that our ability to achieve future growth is dependent in part on our ability to continueeffectively expand into new international markets. In some of our international expansion efforts. However, despite our efforts to do so,markets, we have experienced unexpected difficulties that have resulted in slower than anticipated growth. We may not succeed in growing in our existing international markets, entering new international markets on a

- 16-



timely basis, or achieving profitability in new markets. We must overcome significant regulatory and legal barriers before we can begin marketing in any international market. Also, before marketing commences in a new country or market, it is difficult to assess the extent to which our products and sales techniques will be accepted or successful in any given country. In addition to significant regulatory barriers, we may also encounter problems conducting operations in new markets with different cultures and legal systems from those encountered elsewhere. We may be required to reformulate one or more of our products, including Protandim®, before commencing sales of that product in a given country. Once we have entered a market, we must adhere to the regulatory and legal requirements of that market. We cannot assure you that we willmay not be able to obtain and retain necessary permits and approvals in new markets, or that we willmay have sufficientinsufficient capital to finance our expansion efforts in a timely manner.

Economic conditions, including the current financial crisis and declining consumer confidence and spending,

Inability of new products to gain distributor or market acceptance could harm our business.
In fiscal 2015, we introduced Axio

®, our energy drink mix formulated to promote alertness and support mental performance. We believe our ability to introduce new products that gain acceptance among our distributors and customers is an important part of our ability to grow our revenue in future periods. However, any new products we introduce may not gain distributor and market acceptance to the extent we anticipate or project. Factors that could affect our ability to introduce new products include, among others, government regulations, the inability to attract and retain qualified research and development staff, the termination of third-party research and collaborative arrangements, proprietary protections of competitors that may limit our ability to offer comparable products and the difficulties in anticipating changes in consumer tastes and buying preferences. In addition, new products we introduce may not be successful or generate substantial revenue. The introduction of a new product could also negatively impact other product lines to the extent our distributor leaders focus their efforts on the new product instead of an existing product. If any of our products fail to gain distributor acceptance, we could see an increase in product returns.

Our business could be negatively impacted if we fail to execute our product launch process due to increased pressure on our supply chain, information systems and management.
Although our product launch process may vary by market, we generally introduce new products to our independent distributors and preferred customers through limited-time offers and promotions. The limited-time offers typically generate significant activity and a high level of purchasing, which may result in a higher than normal increase in revenue during the quarter of the limited-time offer and skew year-over-year and sequential comparisons. We may experience difficulty effectively managing growth associated with these limited-time offers. In addition, the size and condensed schedule of these product launches increases pressure on our supply chain. If we are unable to accurately forecast sales levels in each market, obtain sufficient ingredients or produce a sufficient supply to meet demand, we may incur higher expedited shipping costs and we may temporarily run out of stock of certain products, which could negatively impact the enthusiasm of our independent distributors and preferred customers. Conversely, if demand does not meet our expectations for a product launch, we could incur increased inventory write-offs. Any inventory write-off would negatively impact our gross margins. In addition, our order processing systems could have difficulties handling the high volume of orders generated by limited-time offers. Although our previous limited-time offers have not materially affected our product return rate, these events may increase our product return rate in the future.
We rely on our information technology systems to manage numerous aspects of our business, and a disruption in these systems could adversely affect our business.
We depend on our information technology, or IT, systems to manage numerous aspects of our business, including our finance and accounting transactions, to manage our independent distributor compensation plan and to provide analytical information to management. Our IT systems are an essential component of our business and growth strategies, and a serious disruption to our IT systems could significantly limit our ability to manage and operate our business efficiently. These systems are vulnerable to, among other things, damage and interruption from power loss or natural disasters, computer system and network failures, loss of telecommunications services, physical and electronic loss of data, security breaches and computer viruses. Any disruption could cause our business and competitive position to suffer and adversely affect our business and operating results. In addition, if we experience future growth, we will need to scale or change some of our systems to accommodate the increasing number of independent distributors and other customers. For example, we are in the process of implementing a new back office system and mobile application to be used by our independent distributors. The implementation of the new back office system is a complicated process that will take multiple years to complete. In addition, we may not be successful in implementing a mobile application that our independent distributors find useful. Our ability to compete could be harmed if we are unable to successfully implement the new back office system or if our independent distributors do not adapt well to the new system or mobile application.

- 17-



Cyber security risks and the failure to maintain the integrity of data belonging to our company, employees, independent distributors and preferred customers could expose us to data loss, litigation and liability, and our reputation could be significantly harmed.
We collect and retain large volumes of data relating to our business and from our employees, independent distributors and preferred customers for business purposes, including for transactional and promotional purposes, and our various information technology systems enter, process, summarize and report such data. The integrity and protection of this data is critical to our business. We are subject to significant security and privacy regulations, as well as requirements imposed by the credit card industry. Maintaining compliance with these evolving regulations and requirements could be difficult and may increase our expenses. In addition, a penetrated or compromised data system or the intentional, inadvertent or negligent release or disclosure of data could result in theft, loss or fraudulent or unlawful use of data relating to our company or our employees, independent distributors or preferred customers, which could harm our reputation, disrupt our operations, or result in remedial and other costs, fines or lawsuits.
Our credit facility includes debt service obligations and restrictive covenants that could impede our operations and flexibility.
We entered into a Financing Agreement in October 2013 that provides for a credit facility consisting of a term loan facility in an aggregate principal amount of up to $47 million and a delayed draw term loan facility in an aggregate principal amount not to exceed $20 million (the "Financing Agreement"). At the end of the fiscal year ended June 30, 2015, the principal amount owing under the credit facility was approximately $22 million. The principal amount borrowed under the credit facility is repayable in consecutive quarterly installments. We expect to generate the cash necessary to pay the principal and interest on the credit facility from our cash flows provided by operating activities. However, our ability to meet our debt service obligations will depend on our future performance, which may be affected by financial, business, economic, demographic and other factors. If we do not have enough money to pay our debt service obligations, we may be required to refinance all or part of our debt, sell assets, borrow more money or raise cash through the sale of equity. In such an event, we may not be able to refinance our debt, sell assets, borrow more money or raise cash through the sale of equity on terms acceptable to us or at all. Also, our ability to carry out any of these activities on favorable terms, if at all, may be further impacted by any financial or credit crisis which may limit access to the credit markets and increase the cost of capital.
The credit facility is secured by a lien on substantially all of our assets, and the assets of our subsidiaries, and contains customary covenants, including covenants that restrict our ability to incur or guarantee additional indebtedness, pay dividends on and redeem capital stock, make other payments, including investments, sell our assets and enter into consolidations, mergers or transfers of all or substantially all of our assets. The credit facility includes financial covenants that require us to maintain specified financial ratios and satisfy certain financial condition tests. Our ability to meet these financial ratios and tests can be affected by events beyond our control and we may be unable to meet these ratios and tests. A breach of any of the covenants, ratios, tests or restrictions imposed by the credit facility would result in an event of default and the lender could declare all amounts outstanding under the credit facility to be immediately due and payable. Our assets may not be sufficient to repay the indebtedness if the lenders accelerate our repayment of the indebtedness under the credit facility.
We may not be able to comply with the financial covenants set forth in the Financing Agreement.
The Financing Agreement we entered into in October 2013 contains financial covenants that require us to maintain specified financial ratios and satisfy certain financial condition tests. For example, the Financing Agreement originally required us to have a minimum consolidated EBITDA for the four consecutive fiscal quarters ended March 31, 2015 of at least $20.6 million. We were not in compliance with this financial covenant at March 31, 2015 and we entered into Amendment No. 1 to Financing Agreement on May 1, 2015 (the "Amendment") to remedy our noncompliance and to establish a lower EBITDA covenant for the four consecutive fiscal quarters ending March 31, 2015 and June 30, 2015. The Amendment, however, did not revise the required minimum consolidated EBITDA for periods subsequent to June 30, 2015.
On August 27, 2015 we entered into an Amendment No. 2 to Financing Agreement ("Amendment No. 2"). Amendment No. 2 revised the covenants related to minimum consolidated EBITDA (as defined in the amended Financing Agreement) for the four consecutive fiscal quarters ending September 30, 2015, December 31, 2015, March 31, 2016 and June 30, 2016 from $22.2 million, $23.1 million, $24.4 million and $25.6 million, respectively, to $14.5 million, $15.0 million, $17.0 million and $17.5 million, respectively. In addition, Amendment No. 2 requires that we make additional monthly accelerated principal payments on our outstanding term loan in the amount of $0.5 million commencing on October 15, 2015 and continuing until the term loan has been paid in full. Amendment No. 2 also requires that we make additional accelerated payments at the end of each calendar quarter in the amount of all unrestricted cash on hand as of the close of business on the last day of the quarter in excess of $12.5 million. If we are unable to further amend the Financing Agreement or significantly increase our revenue and manage our expenses, our consolidated EBITDA may not exceed the minimum consolidated EBITDA required by the Financing Agreement

- 18-



and, as a result, an event of default would exist under the Financing Agreement for which our lender could accelerate our repayment of the indebtedness.
Our independent distributors could fail to comply with applicable legal requirements or our distributor policies and procedures, which could result in claims against us that could harm our business.
Our independent distributors are independent contractors and, accordingly, we are not in a position to directly provide the same direction, motivation and oversight as we would if distributors were employees. As a result, there can be no assurance that our distributors will participate in our marketing strategies or plans, accept our introduction of new products, or comply with our distributor policies and procedures.
Extensive federal, state, local and international laws regulate our business, products and direct selling activities. Because we have expanded into foreign countries, our policies and procedures for our independent distributors differ slightly in some countries due to the different legal requirements of each country in which we do business. While our distributor policies and procedures are designed to govern distributor conduct, it can be difficult to enforce these policies and procedures because of the large number of distributors and their independent status. Violations by our independent distributors of applicable law or of our policies and procedures in dealing with customers could reflect negatively on our products and operations and harm our business reputation. In addition, it is possible that a court could hold us civilly or criminally accountable based on vicarious liability because of the actions of our independent distributors. In the past, we have had independent distributors investigated by government agencies for conduct violating the law and our policies. This type of investigation can have an adverse effect on us even if we are not involved in the independent distributor's activities.
A substantial portion of our business is conducted in foreign markets, exposing us to the risks of trade or foreign exchange restrictions, increased tariffs, foreign currency fluctuations, disruptions or conflicts with our third party importers and similar risks associated with foreign operations.
A substantial portion of our sales are generated outside the United States. If we are successful in entering additional foreign markets, we anticipate that the percentage of our sales generated outside the United States will increase. There are substantial risks associated with foreign operations. For example, a foreign government may impose trade or foreign exchange restrictions or increased tariffs, which could negatively impact our operations and financial results. We are also exposed to risks associated with foreign currency fluctuations. For instance, in preparing our financial statements, we translate revenue and expenses in our markets outside the United States from their local currencies into U.S. dollars using weighted average exchange rates. If the U.S. dollar strengthens relative to local currencies, our reported revenue, gross profit and net income will likely be reduced. Foreign currency fluctuations can also result in losses and gains resulting from translation of foreign currency denominated balances on our balance sheet. Additionally, purchases from suppliers are generally made in U.S. dollars while sales to distributors are generally made in local currencies. Accordingly, strengthening of the U.S. dollar versus a foreign currency could have a negative impact on us. Specifically, because a significant percentage of our revenues are generated in Japan, strengthening of the U.S. dollar versus the Japanese yen has had and could continue to have an adverse impact on our financial results. Although we may engage in transactions intended to reduce our exposure to foreign currency fluctuations, there can be no assurance that these transactions will be effective. Given the complex global political and economic dynamics that affect exchange rate fluctuations, it is difficult to predict future fluctuations and the effect these fluctuations may have upon future reported results or our overall financial condition.
Additionally, we may be negatively impacted by conflicts with or disruptions caused or faced by third party importers, as well as conflicts between such importers and local governments or regulatory agencies. Our operations in some markets also may be adversely affected by political, economic and social instability in foreign countries.
Global economic conditions have deteriorated significantly over the past several years andcould harm our business.
Global economic conditions continue to be challenging and unpredictable. Consumer confidence and spending have declined drasticallyin recent years and the global credit crisis has limited access to capital for many companies and consumers. The global economic downturn could adversely impact our business in the future by causing a decline in demand for our products, particularly if the economic conditions are prolonged or worsen. In addition, poor global economic conditions may adversely impact access to capital for us and our suppliers, may decrease our independent distributors’ ability to obtain or maintain credit, cards, and may otherwise adversely impact our operations and overall financial condition.

If we are unable to maintain our level of internal controls, our shareholders could lose confidence in our financial reporting and our stock price could suffer.
We have implemented internal controls to help ensure the accuracy of our financial reporting and have implemented internal controls to comply with Section 404 of the Sarbanes-Oxley Act of 2002. We regularly audit our internal controls and various aspects of our business and we regularly assess the effectiveness of our internal controls. There can be no assurance, however,

- 19-



that these internal or external assessments and audits will identify all significant or material weaknesses in our internal controls. Any failure to correct a weakness in internal controls could result in the disclosure of a material weakness. If a material weakness results in a material misstatement in our financial results, we may also have to restate our financial statements.
If we are to expand our product offerings, we may need to raise additional capital.

WeAlthough we introduced additional products in each of fiscal 2014 and 2015, we primarily depend on Protandim® for our revenue. We may decide to expand our product portfolio and may seek to do so by acquiring products by license or through product or company acquisitions. If cash generated from operations is insufficient to satisfy our requirements in this regard, we may need to raise additional capital, which may be dilutive to our existing shareholders. If we are unable to raise additional required capital in a timely manner, we could be forced to significantly reduce our growth plans.

We could be exposed to certain environmental liabilities due to our past operations and property ownership.

During the 1990s, we owned mining properties in the Yaak River mining district of Montana. We never conducted any mining operations or ore processing on these properties, nor have we performed on-site environmental studies on these properties. The State of Montana Department of Environmental Quality believed that the properties may contain residues from past mining. We may be liable for material environmental liabilities associated with these properties.

In addition, until November 2004, we owned land in Lawrence, Colorado. We are not aware of any environmental liabilities with respect to this land. The party that acquired the land from us assumed any environmental liability related to the land. Nonetheless, a governmental agency or a private party could seek to hold us accountable for such environmental liabilities, if any.

In the past, we had material weaknesses in our internal control over financial reporting. If we are unable to maintain our level of internal controls in the future, our shareholders could lose confidence in our financial reporting and our stock price could suffer.

In connection with the preparation of our financial statements included in our Form 10-K for fiscal year 2011, as well as certain other previously issued financial statements, we concluded that there were material weaknesses in

-23-


our internal control over financial reporting. While we were able to remedy these material weaknesses during fiscal 2012, as we expand our business, especially outside of the United States, if we fail to maintain our control procedures, or otherwise comply with Section 404 of the Sarbanes-Oxley Act of 2002, it could negatively affect our business, the price of our common stock and market confidence in our reported financial information.

Risk Factors Relating to ourOur Business and Industry

We primarily depend on a single product for our revenue.

Although we generate revenue through the sale of LifeVantage TrueScienceCanine Health®, our line of LifeVantage TrueScience® skin care products and Axio®, we primarily rely on the sale of our Protandim® product for our revenue. We do not have a broad portfolio of other products that we could rely on to support our operations if we were to experience any difficulty with the manufacture, marketing, sale or distribution of Protandim®. For example, our revenue was adversely impacted because sales of Protandim® slowed following our voluntary product recall during fiscal 2013. If we have similar problems in the future, our results could be negatively affected. In addition, we may be unable to sustain or increase the price or sales levels for Protandim®, which could harm our business.

If we are unable to retain our existing independent distributors or attract additional independent distributors, our revenue will not increase and may even decline.
Our independent distributors may terminate their services at any time, and we can and have in the past terminated distributors for conduct violative of our policies and procedures. As such, like most direct selling companies, we have experienced and are likely to continue to experience turnover among independent distributors. The departure for any reason of one of our leading independent distributors can be a major disruption to other independent distributors and can have a significant negative impact on our operating results. Independent distributors who join our company to purchase our products for personal consumption or for short-term income goals may only stay with us for a short time. While we take steps to help train, motivate, and retain independent distributors, we cannot accurately predict the number or productivity of our independent distributors.
Our operating results will be harmed if we and our independent distributor leaders do not generate sufficient interest in our business to retain existing independent distributors and attract new independent distributors. The number and productivity of our independent distributors could be harmed by several factors, including:
any adverse publicity regarding us, our products, our distribution channel, or our competitors;
lack of interest in existing or new products or their failure to achieve desired results;
lack of a compelling business opportunity sufficient to generate the interest and commitment of new independent distributors;
any changes we might make to our independent distributor compensation plan;
any negative public perception of our company or our products or their ingredients;
any negative public perception of our independent distributors and direct selling business in general;
our actions to enforce our policies and procedures;

- 20-



any efforts to sell our products through competitive channels;
any regulatory actions or charges against us or others in our industry; and
general economic and business conditions.
High quality material for our products may be difficult to obtain or expensive.
Raw materials account for a significant portion of our manufacturing costs and we rely on third-party suppliers to provide raw materials. Suppliers may be unable or unwilling to provide the raw materials our manufacturers need in the quantities requested, at a price we are willing to pay, or that meet our quality standards. We are also subject to potential delays in the delivery of raw materials caused by events beyond our control, including labor disputes, transportation interruptions and changes in government regulations. Our business could be adversely affected if we are unable to obtain a reliable source of any of the raw materials used in the manufacturing of our products that meets our quality standards. Additionally, if demand for our products exceeds our forecasts, we may have difficulties in obtaining additional raw materials in time to meet the excess demand. Any significant delay in or disruption of the supply of raw materials could, among other things, substantially increase the cost of such materials, require reformulation or repackaging of products, require the qualification of new suppliers, or result in our inability to meet customer demands.
Although our independent distributors are independent contractors, improper distributor actions that violate laws or regulations could harm our business.

Distributor

Our independent distributors are not employees and act independent of us. However, activities by our independent distributors that violate applicable laws or regulations could result in government or third partythird-party actions against us, which could harm our business. Our independent distributors are not employees and act independently of us. We implementagree to abide by our strict policies and procedures designed to ensure our independent distributors will comply with legal requirements. We have a compliance department that addresses violations of our independent distributors when they become known to us. However, given the size of our independent distributor force,network, we experience problems with independent distributors violating our policies and procedures from time to time. Ourtime and are not always able to discover or remedy such violations.
One of our most significant areaareas of risk with respect to independent distributor activities relates to improper product claims and claims regarding the business opportunity of being an independent distributor. Any determination by the Federal Trade Commission, any state agency or other similar governmental agency outside the United States that we or our independent distributors are not in compliance with applicable laws could materially harm our business. Even if governmental actions do not result in rulings or orders against us, they could create negative publicity that could detrimentally affect our efforts to recruit or motivate independent distributors and attract customers.customers or lead to consumer lawsuits against us. As we experience growth in the number of our independent distributors, we have seen an increase in sales aids and promotional material being produced by distributors and distributor groups in some markets. This places an increased burden on us to monitor compliance of such materials and increases the risk that such materials could contain problematic product or marketing claims in violation of our policies and applicable regulations. As we expand internationally, our distributors sometimes attempt to anticipate additional new markets that we may enter in the future and begin marketing and sponsoring activities in markets where we are not qualified to conduct business. We could face fines or other legal action if our distributors violate applicable laws and regulations.

We are dependent upon third parties to manufacture our product.
We currently rely on third parties to manufacture the products we sell. We are dependent on the uninterrupted and efficient operation of third party manufacturers’ facilities. We currently have multiple third-party contractors who manufacture Protandim®, however we currently only have one third-party contractor who manufacturers each of Canine Health®, our line of LifeVantage TrueScience® skin care products and Axio®. If weany of our current manufacturers are unable or unwilling to retainfulfill our existing independent distributorsmanufacturing requirements or seek to impose unfavorable terms, we will likely have to seek out other manufacturers, which could disrupt our operations and recruit additional independent distributors, our revenue will not increase and may even decline.

In fiscal 2009, we initiated network marketing sales through which independent distributors enter into agreements with us to sell our products. Our independent distributors may terminate their services at any time, and, like most network marketing companies, we have experienced and are likely to continue to experience turnover among independent distributors. Independent distributors who join our company to purchase our products for personal consumption or for short-term income goals may only stay with us for a short time. While we take steps to help train, motivate, and retain independent distributors, we cannot accurately predict the number or productivity of our independent distributors.

Our operating results will be harmed if we and our independent distributor leaders do not generate sufficient interest in our business to retain existing independent distributors and attract new independent distributors. The number and productivity of our independent distributors could be harmed by several factors, including:

any adverse publicity regarding us, our products, our independent distribution channel, or our competitors;

-24-


lack of interest in existing or new products or their failure to achieve desired results;

lack of a compelling business opportunity sufficient to generate the interest and commitment of new independent distributors;

any changes we might make to our independent distributor compensation plan;

any negative public perception of our products and their ingredients;

any negative public perception of our independent distributors and network marketing businesses in general;

our actions to enforce our policies and procedures;

any efforts to sell our products through competitive channels;

any regulatory actions or charges against us or others in our industry; and

general economic and business conditions.

The dietary supplement market is highly competitive.

The dietary supplements retail market is large and highly competitive and fragmented. Participants include specialty retailers, supermarkets, drugstores, mass merchants, multi-level marketing organizations, on-line merchants, mail-order companies, and a variety of other smaller participants. Many of our competitors have greater financial and other resources available to them and possess better manufacturing, independent distribution and marketing capabilities. We believe that the market is also highly sensitive to the introduction of new products, including various prescription drugs, which may rapidly capture a significant share of the market. Moreover, because of regulatory restrictions concerning claims about the efficacy of dietary supplements, we may have difficulty differentiating our products from our competitors’ products, and competing products entering the dietary supplements market could harm our revenue. In the United States and Japan, we also compete for sales with heavily advertised national brands manufactured by large pharmaceutical and food companies, as well as other retailers. In addition, as some products become more mainstream, we experience increased competition for those products as more participants enter the market. Our international competitors include large international pharmacy chains, major international supermarket chains, and other large U.S.-based companies with international operations. We may not be ablesuccessful in finding alternative manufacturing resources. In addition, competitors who perform their own manufacturing may have an advantage over us with respect to compete effectivelypricing, availability of product, and in other areas through their control of the manufacturing process.

Disruptions to transportation channels used to distribute our attemptproducts may adversely affect our margins and profitability.
We generally rely on the uninterrupted and efficient operation of third-party logistics companies to do sotransport and deliver our products. These third-party logistics companies may experience disruptions to the transportation channels used to distribute our products, including increased airport and shipping port congestion, a lack of transportation capacity, increased fuel expenses, and a shortage of manpower. Disruptions to the transportation channels experienced by our third party logistics companies may result in increased pricing pressure, whichcosts, including the additional use of airfreight to meet demand.

- 21-



We are subject to risks related to product recalls.
We have implemented measures in our manufacturing process that are designed to prevent and detect defects in our products, including contaminants. However, such measures may resultnot prevent or reveal defects or detect contaminants in lower marginsour products and such defects and contaminants may not become apparent until after our products have been sold into the market. Accordingly, there is a risk that product defects will occur, or that our products will contain foreign contaminants, and that such defects and contaminants will require a product recall. We do not maintain product recall insurance. In December 2012, we commenced a voluntary recall of certain lots of Protandim® to alleviate concerns that some tablets may have included small metal fragments. We discovered these small metal fragments in certain batches of turmeric extract, an ingredient in Protandim® we purchase from third-party suppliers. Product recalls and subsequent remedial actions can be expensive to implement and could have a material adverse effect on our business, results of operations and financial condition.

Regulations governing In addition, product recalls could result in negative publicity and public concerns regarding the production and marketingsafety of our personal care productproducts, either of which could harm the reputation of our business.

LifeVantage TrueScience®,products and our anti-aging skin carebusiness and could cause the market value of our common stock to decline.

The events that lead to and followed our voluntary product is subjectrecall in December 2012 strained our relationships with some of our third-party manufacturers. Additionally, following the voluntary recall we implemented more stringent measures, including several redundant measures, in our manufacturing process to various domesticdetect contaminates. Third-party manufacturers may be reluctant to implement these redundant measures, may refuse to manufacture our products, and foreign lawsthese additional measures may increase our cost of goods sold and further strain our relationships with manufacturers.
Laws and regulations may prohibit or severely restrict direct selling and cause our revenue and profitability to decline, and regulators could adopt new regulations that regulate cosmetic products and set forth regulations for determining whether a product can be marketed as a “cosmetic” or requires further approval as an over-the-counter drug. A determination that LifeVantage TrueScience® impacts the structure or function of the human body, or improper marketing claims bynegatively impact our distributors may lead to a determination that LifeVantage TrueScience® requires pre-market approval as a drug. Such regulations in any given market can limit our ability to import products and can delay product launches as we go through the registration and approval process for those products. Furthermore, if we fail to comply with these regulations, we could face enforcement action against us and we could be fined, forced to alter or stop selling LifeVantage TrueScience® and/or be required to adjust our operations. Our operations also could be harmed if new laws or regulations are enacted that restrict our ability to market or distribute LifeVantage TrueScience® or impose additional burdens or requirements on the contents of our personal care product or require us to reformulate our product.

Network marketing is heavily regulated.

business.

Various government agencies throughout the world regulate network marketingdirect selling practices. The laws and regulations applicable to us and our independent distributors in Japan are particularly stringent. These laws and regulations are generally intended to prevent fraudulent or deceptive schemes, often referred to as “pyramid”

-25-


schemes, which compensate participants primarily for recruiting additional participants irrespectivewithout significant emphasis on the sale of product sales, use high pressure recruiting methodsto end consumers. The laws and regulations in some of our markets impose cancellations, product returns, inventory buy-backs and cooling-off rights for our independent distributors and customers. Excessive refunds and/or do not involve legitimate products.product returns pursuant to local laws and regulations could have a negative impact on our operating results. Complying with these rules and regulations can be difficult and requires the devotion of significant resources on our part. We may not be able to continue business in existing markets or commence operations in new markets if we are unable to comply with these laws or adjust to changes in these laws.

Unfavorable publicity could materially harm our business.
We are highly dependent upon consumers' perceptions of the safety, quality, and efficacy of our products, as well as competitive products distributed by other companies. In the past, we have experienced negative publicity that has harmed our business. Critics of our industry and other individuals whose interests are not aligned with our interests, have in the past and may in the future utilize the Internet, the press and other means to publish criticism of the industry, our company, our products and our competitors, or make allegations regarding our business and operations, or the business and operations of our competitors. For instance, several prominent companies in our industry have been targeted by short sellers who profit if a company's stock price decreases. One such company has been targeted by a short seller who, after taking a significant short position, publicly made allegations regarding the legality of the company's direct selling model. Short sellers have an incentive to publicly criticize our industry and business model and any such criticism may adversely affect our stock price.
Future scientific research or publicity may not be favorable to our industry or any particular product, including Protandim®. Because of our dependence upon consumer perceptions, adverse publicity associated with illness or other adverse effects resulting or claimed to have resulted from the consumption or use of our products or any similar products distributed by other companies could have a material adverse impact on us. Such adverse publicity could arise even if the claims are unsubstantiated or if the adverse effects associated with such products resulted from failure to consume or use such products as directed. Adverse publicity could also increase our product liability exposure, result in increased regulatory scrutiny and lead to the initiation of private lawsuits.
Our direct selling program could be found to be not in compliance with current or newly adopted laws or regulations in one or more markets, which could prevent us from conducting our business in these markets and harm our financial condition and operating results.
Some of the legal and regulatory requirements concerning the direct selling business model are ambiguous and subject to interpretation. As a result, regulators and courts have discretion in their application of these laws and regulations, and the enforcement or interpretation of these laws and regulations by governmental agencies or courts can change. Recent allegations by short sellers regarding the legality of multi-level marketing companies generally have also created intense public scrutiny of our industry and could cause governmental agencies to change their enforcement and interpretation of applicable laws and

- 22-



regulations. The failure of our business to comply with current or newly adopted regulations or interpretations could negatively impact our business in a particular market or in general and may adversely affect our share price.
We may become involved in legal proceedings that are expensive, time consuming and, if adversely adjudicated or settled, could adversely affect our financial results.
Litigation claims can be expensive and time consuming to bring or defend against and could result in settlements or damages that could significantly affect our financial results. It is not possible to predict the final resolution of litigation which we may in the future become party to; the impact of certain of these matters on our business, results of operations and financial condition could be material.
We are currently involved in various lawsuits, both as a plaintiff and as defendant. While we believe the suits against us are without merit, they are quite costly to defend and we cannot be assured that we will ultimately prevail. If we do not prevail and are required to pay damages, it could harm our business.
Government authorities may question our tax positions or transfer pricing policies or change their laws in a manner that could increase our effective tax rate or otherwise harm our business.
As a U.S. company doing business in international markets through subsidiaries, we are subject to various tax and intercompany pricing laws, including those relating to the flow of funds between our company and our subsidiaries. From time to time, we are audited by tax regulators in the United States and in our foreign markets. If regulators challenge our tax positions, corporate structure, transfer pricing mechanisms or intercompany transfers, we may be subject to fines and payment of back taxes, our effective tax rate may increase and our operations may be harmed. Tax rates vary from country to country, and, if tax authorities determine that our profits in one jurisdiction may need to be increased, we may not be able to fully utilize all foreign tax credits that are generated, which will increase our effective tax rate. For example, our federal corporate income tax rate in the United States is 35%. If our profitability in a higher tax jurisdiction, such as Japan where our tax rate in fiscal 2015 was approximately 37%, increases disproportionately to the rest of our business, our effective tax rate may increase. The various customs, exchange control and transfer pricing laws are continually changing and are subject to the interpretation of government agencies. We may experience increased efforts by customs authorities in foreign countries to reclassify our products or otherwise increase the level of duties we pay on our products. Despite our efforts to be aware of and comply with such laws, and changes to and interpretations thereof, there is a risk that we may not continue to operate in compliance with such laws. We may need to adjust our operating procedures in response to such changes and, as a result, our business may suffer. In addition, due to the international nature of our business, we are subject from time to time to reviews and audits by taxing authorities of other jurisdictions in which we conduct business throughout the world.
Our business is subject to strict government regulations.

The manufacturing, packaging, labeling, advertising, sale and distribution of our products are subject to federal laws and regulation by one or more federal agencies, including, in the United States, the FDA, the FTC, the Consumer Product Safety Commission, the United States Department of Agriculture, and the Environmental Protection Agency. These activities are also regulated by various state, local, and international laws and agencies of the states and localities in which our products are sold. For instance, the FDA regulates, among other things, the composition, safety, labeling, and marketing or dietary supplements (including vitamins, minerals, herbs and other dietary ingredients for human use). Government regulations may prevent or delay the introduction, or require the reformulation, of our products, which could result in lost revenues, and increased costs to us.and delay our expansion into new international markets. For instance, the FDA regulates, among other things, the composition, safety, labeling, and marketing of dietary supplements (including vitamins, minerals, herbs, and other dietary ingredients for human use).

The FDA may determine that a particular dietary supplement or ingredient is adulterated or misbranded or both, and may determine that a particular claim or statement of nutritional value that we make to support the marketing of a dietary supplement is an impermissible drug claim, is not substantiated, or is an unauthorized version of a “health claim.” Determining whether a claim is improper frequently involves a degree of subjectivity. Any of these actionsdeterminations by the FDA could prevent us from marketing that particular dietary supplement product, or making certain claims for that product. The FDA could also require us to remove a particular product from the market. Any future recall or removal would result in additional costs to us, including lost revenues from any product that we are required to remove from the market, which could be material. Any product recalls or removals could also lead to liability, substantial costs, and reduced growth prospects.

Additional or more stringent regulations of dietary supplements and other products have been considered from time to time. In recent years, there has been increased pressure in the United States and other markets to increase regulation of dietary supplements. New regulations could impose additional restrictions, including requiring reformulation of some products to meet new standards, recalls or discontinuance of some products not able to be reformulated, additional record-keeping requirements, increased documentation of the properties of some products, additional or different labeling, additional scientific substantiation,

- 23-



additional adverse event reporting, or other new requirements. Any of these developments could increase our costs significantly. In the United States, for example, some legislators and industry critics continue to push for increased regulatory authority by the FDA over nutritional supplements. Our business could be harmed if more restrictive legislation is successfully introduced and adopted in the future. In the United States, the FTC’s Guides Concerning the Use of Endorsements and Testimonials in Advertising, or Guides, require disclosure of material connections between an endorser and the company they are endorsing and generally do not allow marketing using atypical results. Our independent distributors have historically used testimonials to market and sell Protandim®.our products. Producing marketing materials that conform to the requirements and restrictions of the Guides may diminish the impact of our marketing efforts and negatively impact our sales results. If we or our distributors fail to comply with these Guides, the FTC could bring an enforcement action against us and we could be fined and/or forced to alter our marketing materials. Our operations also could be harmed if new laws or regulations are enacted that restrict our ability to market or distribute nutritional supplements or impose additional burdens or requirements on nutritional supplement companies or require us to reformulate our products.

In addition, the Dietary Supplement and Nonprescription Drug Consumer Protection Act which was passed by Congress in 2006, imposes significant regulatory requirements on dietary supplement manufacturers,supplements, packers and distributors including the reporting of “serious adverse events” to the FDA and recordkeepingrecord keeping requirements. Complying with this legislation could raise our costs and negatively impact our business. We and our suppliers are also required to comply with FDA regulations with respect to Currentcurrent Good Manufacturing ProceduresPractices in manufacturing, packaging, or holding dietary ingredients and dietary supplements. These regulations require

-26-


dietary supplements to be prepared, packaged, and held in compliance with procedures that we and our subcontractors must develop and make available for inspection by the FDA. These regulations could raise our costs and negatively impact our business. Additionally, our third-party suppliers or vendors may not be able to comply with these rules without incurring substantial expenses. If our third-party suppliers or vendors are not able to comply with these rules, we may experience increased cost or delays in obtaining certain raw materials and third-party products. In 2011, the FDA published draft guidance which is intended, among other things, to help manufacturers and distributors of dietary supplement products determine when they are required to file with the FDA a New Dietary Ingredient, or NDI, notification with respect to a dietary supplement product. In this draft guidance, the FDA highlighted the necessity for marketers of dietary supplements to submit NDI notifications as an important preventive control to ensure that consumers are not exposed to potential unnecessary public health risks in the form of new ingredients with unknown safety profiles. Although we do not believe that Protandim® contains an NDI, if the FDA were to conclude that we should have filed an NDI notification for Protandim®, then we could be subject to enforcement actions by the FDA. Such enforcement actions could include product seizures and injunctive relief being granted against us, any of which would harm our business.

Regulations governing the production and marketing of our line of skin care products could harm our business.
LifeVantage TrueScience®, our line of anti-aging skin care products, is subject to various domestic and foreign laws and regulations that regulate cosmetic products and set forth regulations for determining whether a product can be marketed as a “cosmetic” or requires further approval as a drug. A determination that our skin care products impact the structure or function of the human body, including due to improper marketing claims by our independent distributors may lead to a determination that the LifeVantage TrueScience® skin care products require pre-market approval as a drug. Such regulations in any given market can limit our ability to import products and can delay product launches as we go through the registration and approval process for those products. Furthermore, if we fail to comply with these regulations, we could face enforcement action against us and we could be fined, forced to alter or stop selling our skin care products and/or be required to adjust our operations. Our operations also could be harmed if new laws or regulations are enacted that restrict our ability to market or distribute our skin care products or impose additional burdens or requirements on the contents of our personal care products or require us to reformulate our products.
We are subject to the risk of investigatory and enforcement action by the FTC.

We will always beare subject to the risk of investigatory and enforcement action by the FTC based on our advertising claims and marketing practices. The FTC routinely reviews product advertising, including websites, to identify significant questionable advertising claims and practices. The FTC has brought many actions against dietary supplement companies based upon allegations that applicable advertising claims or practices were deceptive or not substantiated. If the FTC initiates an investigation, the FTC can initiate pre-complaint discovery that may be nonpublic in nature. Any investigation may be very expensive to defend and may result in an adverse ruling or in a consent decree.

Unfavorable publicity

Non-compliance with anti-corruption laws could materially harm our business.

We

Our international operations are highly dependent upon consumers’ perceptionssubject to anti-corruption laws, including the Foreign Corrupt Practices Act, also known as the FCPA. Any allegations that we are not in compliance with anti-corruption laws may require us to dedicate time and resources to an internal investigation of the safety, quality,allegations or may result in a government investigation. Any determination that our operations or activities are not in compliance with existing anti-corruption laws or regulations could result in the imposition of substantial

- 24-



fines, and efficacyother penalties. Although we have implemented anti-corruption policies and controls to protect against violation of these laws, we cannot be certain that these efforts will be effective.
If we are unable to build and integrate our new management team, our business could be harmed.
Since February 2015, our executive management team has undergone significant change, including the termination or resignation from employment of each of our products,former President and Chief Executive Officer, Chief Financial Officer, Chief Sales Officer, Chief Science Officer and General Counsel. In addition, in May 2015, Darren Jensen joined our company as our new President and Chief Executive Officer; in July 2015, Justin Rose was appointed as our Chief Sales Officer and in August 2015, Mark Jaggi became our Chief Financial Officer.
Our success depends largely on the development and execution of our business strategy by our senior management team. Each of our President and Chief Executive Officer, Chief Sales Officer and Chief Financial Officer is new to our Company and none of them have worked together in the recent past. We cannot assure you that our new management will succeed in working together as a team, working well with our other existing employees or successfully executing our business strategy in the near-term or at all, which could harm our business and financial prospects. Further, integrating new management into existing operations may be challenging. If we are unable to effectively integrate our new executive management team, our operations and prospects could be harmed.
The loss of or inability to attract key personnel could negatively impact our business.
Our future performance will depend upon our ability to attract, retain, and motivate our executive and senior management team and scientific staff. Our success depends to a significant extent both upon the continued services of our current executive and senior management team and scientific staff, as well as competitive products distributed by other companies. Inour ability to attract, hire, motivate, and retain additional qualified management and scientific staff in the pastfuture. Specifically, competition for executive and senior staff in the direct selling and dietary supplement markets is intense, and our operations could be adversely affected if we have experienced negative publicity that has harmed our business. Criticscannot attract and retain qualified personnel. Additionally, former members of our industryexecutive and other individuals who want to pursue an agenda,senior management team have in the past, and maycould join in the future utilizeor form companies that compete against us in the internet,direct selling industry.
All of our employees are “at will” employees, which means any employee may quit at any time and we may terminate any employee at any time. We do not carry “key person” insurance covering members of senior management or our employees.
We may be held responsible for certain taxes or assessments relating to the pressactivities of our independent distributors, which could harm our financial condition and operating results.
Our distributors are subject to taxation, and in some instances, legislation or governmental agencies impose an obligation on us to collect taxes, such as value added taxes, and to maintain appropriate records. In the event that local laws and regulations or the interpretation of local laws and regulations change to require us to treat our independent distributors as employees, or that our distributors are deemed by local regulatory authorities in one or more of the jurisdictions in which we operate to be our employees rather than independent contractors under existing laws and interpretations, we may be held responsible for social security and related taxes in those jurisdictions, plus any related assessments and penalties, which could harm our financial condition and operating results. If our distributors were deemed to be employees rather than independent contractors, we would also face the threat of increased vicarious liability for their actions.
The dietary supplement market is highly competitive.
Our flagship product, Protandim®, competes in the dietary supplements market, which is large, highly competitive and fragmented. Participants include specialty retailers, supermarkets, drugstores, mass merchants, multi-level marketing organizations, on-line merchants, mail-order companies, and a variety of other smaller participants. Many of our competitors have greater financial and other meansresources available to publish criticismsthem and possess better manufacturing, independent distribution and marketing capabilities than we do. We believe some of the industry, our company, ourthese competitors with greater resources are currently working on developing and releasing products and our competitors, or make allegations regarding our business and operations, or the business and operations of our competitors. Future scientific research or publicity may not be favorable to our industry or any particular product, includingthat will compete directly with Protandim®. Because and be marketed as Nrf2 activators. One or more of our dependence upon consumer perceptions, adverse publicity associated with illness or other adverse effects resulting or claimed to have resulted fromthese products could significantly reduce the consumption or use of our product or any similar products distributed by other companies coulddemand for Protandim® and have a material adverse impacteffect on us. Such adverse publicityour revenue. We believe that the market is also highly sensitive to the introduction of new products, including various prescription drugs, which may rapidly capture a significant share of the market. Moreover, because of regulatory restrictions concerning claims about the efficacy of dietary supplements, we may have difficulty differentiating our products from our competitors’ products, and competing products entering the dietary supplements market could arise even ifharm our revenue. In the claims are unsubstantiated or if the adverse effects associatedUnited States and Japan, we also compete for sales with suchheavily advertised national brands manufactured by large pharmaceutical and food companies, as well as other retailers. In addition, as some products resulted from failure to consume or use suchbecome more mainstream, we experience increased competition for those products as directed. Adverse publicity could also increasemore participants enter the market. Our international competitors include large international pharmacy chains, major international supermarket chains, and other large U.S.-based companies with international operations. We may not be able to

- 25-



compete effectively and our product liability exposure,attempt to do so may result in increased regulatory scrutinypricing pressure, which may result in lower margins and lead to the initiationhave a material adverse effect on our results of private lawsuits.

operations and financial condition.

Our intellectual property rights are valuable, and any inability to protect them could reduce the value of our products and brand.

The loss of our intellectual property rights in our products could permit our competitors to manufacture their own version of our products. We have attempted to protect our intellectual property rights in our products through a combination of patents, patent applications, confidentiality agreements, non-compete agreements and other contractual protection mechanisms, and we will continue to do so. While we intend to defend against any threats to our intellectual property, there can be no assurance that our patents or various contractual protections agreements willmay not adequately protect our intellectual property. In addition, we could be required to expend significant resources to defend our rights to proprietary information, and may not be successful in such defense.

-27-


Moreover, our intellectual property rights are more limited outside of the United States than they are in the United States. As such, we cannot assure you that we willmay not be successful in preventing third parties from copying or misappropriating our intellectual property. There can also be no assurance that pending patent applications owned by us will result in patents being issued to us, that patents issued to or licensed by us in the past or in the future will not be challenged or circumvented by competitors or that such patents will be found to be valid or sufficiently broad to protect our products or to provide us with any competitive advantage. Third parties could also obtain patents that may require us to negotiate to obtain licenses to conduct our business, and any required licenses may not be available on reasonable terms or at all. We also rely on confidentiality and non-compete agreements with certain employees, independent distributors, consultants and other parties to protect, in part, trade secrets and other proprietary rights. There can be no assurance that these agreements will not be breached, that we will have adequate remedies for any breach, that others will not independently develop substantially equivalent proprietary information or that third parties will not otherwise gain access to our trade secrets or proprietary knowledge.

Third parties might claim that we infringe on their intellectual property rights.

Although the dietary supplement industry has historically been characterized by products with naturally occurring ingredients, recently it is becoming more common for suppliers and competitors to apply for patents or develop proprietary technologies and processes. Third parties may assert intellectual property infringement claims against us despite our efforts to avoid such infringement. Such claims could prevent us from offering competitive products or result in litigation or threatened litigation.

Challenges by regulatory authorities or private parties to the form of our network marketing system or other regulatory compliance issues could harm our business.

Both regulatory authorities and private parties, including our independent distributors, may challenge the form of our network marketing sales channel or elements of our network marketing system. Adverse rulings in any case filed against a network marketing company, even if it is not against us, could negatively impact our business if they create adverse publicity, modify current regulatory requirements in a manner that is inconsistent with our current business practices, or impose fines or other penalties.

Raw material for our product may be difficult to obtain or expensive.

Raw materials account for a significant portion of our manufacturing costs. Suppliers may be unable or unwilling to provide the raw materials our manufacturers need in the quantities requested, at a price we are willing to pay, or that meet our quality standards. We are also subject to potential delays in the delivery of raw materials caused by events beyond our control, including labor disputes, transportation interruptions and changes in government regulations. Any significant delay in or disruption of the supply of raw materials could, among other things, substantially increase the cost of such materials, require reformulation or repackaging of products, require the qualification of new suppliers, or result in our inability to meet customer demands.

We are dependent upon third parties to manufacture our product.

We currently rely on third parties to manufacture the products we sell. We are dependent on the uninterrupted and efficient operation of third party manufacturers’ facilities. If any of our current manufacturers are unable to fulfill our manufacturing requirements or seek to impose unfavorable terms, we will likely have to seek out other manufacturers, which could disrupt our operations and we may not be successful in finding alternative manufacturing resources. In addition, competitors who perform their own manufacturing may have an advantage over us with respect to pricing, availability of product, and in other areas through their control of the manufacturing process.

-28-


Our business is susceptible to product liability claims.

The manufacture and sale of any product for human consumption raises the risk of product liability claims. These claims may derive from the product itself or a contaminant found in the product from the manufacturing, packaging, sales process or even due to tampering by unauthorized third parties. Our products consist of vitamins, minerals, herbs, and other ingredients that are classified as foods or dietary supplements and are not subject to pre-market regulatory approval in the United States. Our products could contain contaminated substances, and some of our products contain ingredients that do not have long histories of human consumption. Previously unknown adverse reactions resulting from human consumption of these ingredients could occur. In addition, third-party manufacturers produce manyall of the products we sell. As a distributor of products manufactured by third parties, we may also be liable for various product liability claims for these products we dodespite not manufacture.manufacturing them. We may be subject to various product liability claims, including, among others, that our products include inadequate instructions for use or inadequate warnings concerning possible side effects and interactions with other substances. Any product liability claim against us could result in increased costs and could adversely affect our reputation with our customers, which in turn could adversely affect our revenues and operating income. Although we maintain insurance coverage, there is a risk that our insurance will not cover our potential exposure completely or would fail to cover a particular claim, in which case we may not have the financial resources to satisfy such claim. In addition, certain types of damages, such as punitive damages, are not covered by our insurance policy.

We may become involved in legal proceedings that are expensive, time consuming and, if adversely adjudicated or settled, could adversely affect our financial results.

Litigation claims can be expensive and time consuming to bring or defend against and could result in settlements or damages that could significantly affect our financial results. It is not possible to predict the final resolution of the litigation to which we may in the future become party to, and the impact of certain of these matters on our business, results of operations and financial condition could be material.

The loss of key personnel could negatively impact our business.

Our future performance will depend upon our ability to attract, retain, and motivate our executive and senior management team and scientific staff. Our success depends to a significant extent both upon the continued services of our current executive and senior management team and scientific staff, as well as our ability to attract, hire, motivate, and retain additional qualified management and scientific staff in the future. In addition, competition for executive and senior staff in the dietary supplement market is intense, and our operations could be adversely affected if we cannot attract and retain qualified personnel.

All of our employees are “at will” employees, which means any employee may quit at any time and we may terminate any employee at any time. We do not carry “key person” insurance covering members of senior management or scientific staff.

Economic, political, and other risks associated with our international operations could adversely affect our revenues and international growth prospects.

As part of our business strategy, we intend to continue to expand our international presence. Our international operations are subject to a number of risks inherent to operating in foreign countries, and any expansion of our international operations will increase the effects of these risks. These risks include, among others:

political and economic instability of foreign markets;

foreign governments’ restrictive trade policies;

lack of well-established or reliable legal systems in certain areas in which we operate;


- 26-



inconsistent product regulation or sudden policy changes by foreign agencies or governments;

-29-


the imposition of, or increase in, duties, taxes, government royalties, or non-tariff trade barriers;

difficulty in collecting international accounts receivable and potentially longer payment cycles;

the possibility that a foreign government may limit our ability to repatriate cash;

increased costs in maintaining international marketing efforts;

problems entering international markets with different cultural bases and consumer preferences; and

fluctuations in foreign currency exchange rates.

Any of these risks could have a material adverse effect on our international operations and our growth strategy.

Risks Related to Ownership of Our Common Stock

If

The failure to maintain compliance with the holderscontinued listing standards of the Nasdaq Capital Market could result in delisting and adversely affect the market price and liquidity of our outstanding warrants and options exercise their securities for shares ofcommon stock.
Our common stock is currently listed on the Nasdaq Capital Market. To maintain our listing on the Nasdaq Capital Market we will issue upare required to 24,071,230 shares,meet its continued listing standards, including, among others, Nasdaq Listing Rule 5550(a)(2), which will materially dilute the voting powerrequires listed securities to maintain a minimum closing bid price of our currently outstanding common stock and could cause our stock price to decline.

As of June 30, 2012,$1.00 per share (the “Bid Price Rule”).

On April 1, 2015, we received a written notice from Nasdaq notifying us that we had 110,174,030 sharesnot been in compliance with the Bid Price Rule for a period of common stock outstanding. As of June 30 2012, we also had outstanding warrants that are exercisable for an aggregate of 12,964,234 shares of common stock and stock options outstanding for an aggregate of 11,106,996 shares of common stock.consecutive days. The issuance of these shares will dilutenotice has no immediate effect on the voting power of our currently outstanding common stock and could cause our stock price to decline.

The market price of our securities could be adversely affected by sales of restricted securities.

Actual sales or the prospect of future sales of shareslisting of our common stock underon the Nasdaq Capital Market. In accordance with Nasdaq Listing Rule 144 may5810(c)(3)(A), we have a depressive effect uponperiod of 180 days from the pricedate of and market for, our common stock. In addition, the shares of common stock we may issue upon the exercise of warrants described above may also be sold inwritten notice, or until September 28, 2015, to regain compliance with the Bid Price Rule. To regain compliance with the Bid Price Rule, 144. We cannot predict what effect, if any, that sales of shares of common stock, or the availability of these shares for sale, will have on the market prices prevailing from time to time. Historically, the trading volumeclosing bid price of our common stock has been lowmust meet or exceed $1.00 per share for a minimum of ten consecutive business days during the 180 day compliance period. If we do not regain compliance with the Bid Price Rule during the compliance period ending September 28, 2015, we may be afforded a second compliance period of 180 days if we (i) meet the continued listing requirement for market value of publicly-held shares and all other initial listing standards for the Nasdaq Capital Market, with the exception of the Bid Price Rule, and (ii) notify Nasdaq of our intent to cure the deficiency.

We may be unable to regain compliance with the Bid Price Rule during the compliance period(s), in which case we anticipate Nasdaq will commence proceedings to delist our common stock from the Nasdaq Capital Market. If our common stock is delisted, trading of our common stock most likely will be conducted in the over-the-counter market on an electronic bulletin board established for unlisted securities, such as the OTC Bulletin Board. Such trading would likely reduce the market may not be ableliquidity of our common stock. As a result, an investor would find it more difficult to absorbdispose of, or obtain accurate quotations for the saleprice of, a substantial number of shares. In addition, the possibility that substantial amounts of common stock may be sold in the public market may adversely affect prevailing prices for our common stock and the price of our common stock could impair our ability to raise capital in the future through the sale of equity securities.

decline significantly.

Our stock price may experience future volatility.

The trading price of our common stock has historically been subject to wide fluctuations. The price of our common stock may fluctuate in the future in response to quarter-to-quarter variations in operating results, material announcements by us or competitors, governmental regulatory action, conditions in the dietary supplement industry, or other events or factors, many of which are beyond our control, and some of which do not have a strong correlation to our operating performance.

Our common stock has historically been illiquid.

The average daily trading volume of our common stock on the over-the-counter market was approximately 406,000 and 294,000 shares per day over the fiscal years ended June 30, 2012 and 2011, respectively. If limited trading in our stock continues, it may be difficult for investors to sell their shares in the public market at any given time at prevailing prices.

Substantial sales of shares may impact the market price of our common stock.

stock.

If our shareholders sell substantial amounts of our common stock, the market price of our common stock may decline. These sales also might make it more difficult for us to sell equity or equity-related securities in the future at a time and price that we consider appropriate.

-30-

We would issue up to 3.8 million shares if the holders of our outstanding warrants and options exercise their securities for shares of common stock, which would materially dilute the voting power of our currently outstanding common stock and could cause our stock price to decline.
As of June 30, 2015, we had 97.7 million shares of common stock outstanding. As of June 30, 2015, we also had outstanding warrants that are exercisable for an aggregate of 0.6 million shares of common stock and stock options outstanding for an aggregate of 3.2 million shares of common stock. The issuance of these shares will dilute the voting power of our currently outstanding common stock and could cause our stock price to decline.

- 27-



We have never paid dividends on our capital stock, and we do not currently anticipate paying any cash dividends in the foreseeable future.

We have paid no cash dividends on any of our classes of capital stock to date. Although during fiscal year 20122015 we paid an aggregate of $976,073$9.9 million to repurchase 678,9267.6 million shares of our common stock, we currently intend to retain our future earnings, if any, to fund the development and growth of our business. In addition,Additionally, the terms of any future debt or credit facility, if any, may preclude us from payingFinancing Agreement we entered into in October 2013 contains a customary covenant that restricts our ability to pay dividends. As a result, capital appreciation, if any, of our common stock is likely to be your sole source of gain for the foreseeable future.

When considering the forgoing risk factors, you should keep in mind the cautionary statements in this report and the documents incorporated by reference. We have no obligation and do not undertake to update or revise any such forward-looking statements to reflect events or circumstances after the date of this report.

ITEM 1B — UNRESOLVED STAFF COMMENTS

We do not have any unresolved comments issued by the SEC staff.

None.
ITEM 2 — PROPERTIES

Corporate Offices

During fiscal year 2014, we moved into our corporate headquarters located at 9785 South Monroe Street, Suite 300, Sandy, Utah 84070. The term of the lease for our corporate headquarters is for a term of ten years commencing on February 10, 2015, with an option for us to terminate the lease in our discretion after seven years. The lease includes approximately 44,353 square feet with options to occupy additional space in the future if needed.
In April 2014, we amended the lease for our previous corporate headquarters located at 9815 South Monroe Street in Sandy, Utah, is for 66 months andto reduct the size of this location to approximately 8,742 square feet. In June 2015, we have approximately 20,900 rentable square feet of office space.subleased this location. The lease term began in January 2012 andfor the 9815 South Monroe Street property expires in June 2022.

We lease approximately 3,200 square feet of office space in San Diego, California under a 5-year lease which commenced in November of 2008.

2017.

Our subsidiary, LifeVantage Japan K.K., leases approximately 10,400 square feet of office space located in Tokyo, Japan. The term of the lease is for five years commencingexpiring on August 1, 2012.

2017.

Warehouse Facilities

In September 2009

Since fiscal year 2010, IntegraCore, LLC has provided fulfillment services to us, including services relating to procurement, warehousing, ordering, processing and shipping. We have also entered into arrangements to receive similar services in some of our international markets.
ITEM 3 — LEGAL PROCEEDINGS
On April 9, 2013, we were sued in the Third Judicial District Court for Salt Lake County, State of Utah. The plaintiff in the lawsuit is Ronald Jones, an independent distributor with our company. The lawsuit alleges that we entered into an arrangementagreement with Integracore Fulfillment in Salt Lake City, Utah for assembling distributor kits and fulfillmentMr. Jones related to our network marketing sales channel.his distributor activities in Hong Kong and that we subsequently breached that agreement. It also alleges that we misappropriated trade secrets that purportedly belong to Mr. Jones. The lawsuit seeks over $20 million in damages. We recently expanded our arrangement with Integracore Fulfillmentbelieve the allegations made by Mr. Jones are completely without merit and we now useintend to vigorously defend the lawsuit.
On November 20, 2013, we filed a second regional locationcomplaint in the United States District Court, District of Integracore FulfillmentUtah, Central Division naming Jason Domingo and Ovation Marketing Group, Inc. as defendants. Ovation Marketing Group, Inc. is a former distributor of our company. In the complaint, we allege the defendants breached a contract and misappropriated our trade secrets. On January 21, 2014, the defendants filed an answer and counterclaim in Atlanta, Georgia for priceresponse to our complaint. The defendants' answer and shipping efficiencies. There is no long term agreement relatedcounterclaims allege defamation and tortious interference with economic relations, which the defendants claim resulted in damages of not less than $20 million. We believe the counterclaims alleged by the defendants are completely without merit and we intend to the arrangements with Integracore Fulfillment.

vigorously defend against them.

ITEM 3 — LEGAL PROCEEDINGS

From time to time we are involved in routine litigation. We regularly review all pending litigation matters and establish reserves deemed appropriate by management for these matters when probable loss is estimable. We may become subject to product liability claims. These claims to date have not been material.

ITEM 4 — MINE SAFETY DISCLOSURES

Not applicable.

-31-


PART II

ITEM 5 — MARKET FOR REGISTRANT’S COMMON EQUITY, RELATED STOCKHOLDER MATTERS AND ISSUER PURCHASES OF EQUITY SECURITIES

Market Information and Holders

Since February 2, 2007, our

Our common stock has beenbegan trading on the NASDAQ Capital Market ("NASDAQ") under the symbol "LFVN" in September 2012. Our common stock was previously quoted on the OTC Bulletin Board under the symbol “LFVN.” From October 5, 2004 to February 1, 2007, our common stock was quoted on the OTC Bulletin Board under the symbol “LFLT.”


- 28-



The table below sets forth, for the fiscal quarters indicated, the reported high and low prices of our common stock, as quoted on NASDAQ or the OTC Bulletin Board.Board, as applicable. These prices were reported by an online service, reflect inter-dealer prices, without retail mark-up, mark-down or commission and may not represent actual transactions. Our fiscal year-end is June 30.

   Fiscal year 
   2012   2011 
   High   Low   High   Low 

First Quarter

  $1.69    $1.28    $0.65    $0.42  

Second Quarter

  $1.60    $1.32    $0.50    $0.30  

Third Quarter

  $3.98    $1.33    $0.90    $0.37  

Fourth Quarter

  $3.88    $2.25    $2.07    $0.72  

 Fiscal year
 2015 2014
 High Low High Low
First Quarter$1.55
 $1.12
 $2.68
 $2.13
Second Quarter$1.43
 $1.10
 $2.62
 $1.37
Third Quarter$1.34
 $0.70
 $1.67
 $1.10
Fourth Quarter$0.80
 $0.48
 $1.51
 $1.22
Our common stock is issued in registered form and the following information is taken from the records of our current transfer agent, Computershare Trust Company, Inc., located in Golden, Colorado. As of June 30, 2012,2015, we had 309269 shareholders of record and 110,174,03097.8 million shares of common stock outstanding. This does not include an unknown number of persons who hold shares in street name through brokers and dealers in street name and who are not listed on our shareholder records.

Stock Performance Graph
The following line graph and table compares the cumulative total shareholder return on our common stock with the cumulative total return of (i) the NASDAQ Composite Index and (ii) a market-weighted index of publicly-traded peer companies (the "Peer Group") for the period from June 30, 2010 through June 30, 2015. The data shown assumes an investment on June 30, 2010 of $100 and reinvestment of all dividends into additional shares of the same class of equity, if applicable, to the stock or index. There is no expectation that the rate of return achieved in the prior 5 years will be achievable in the upcoming years.

- 29-



The Peer Group consists of the following companies, which compete in our industry and product categories: Nature's Sunshine Products, Inc.; Nu Skin Enterprises, Inc.; Mannatech, Incorporated; Herbalife LTD.; Reliv International, Inc.; Avon Products, Inc.; USANA Health Sciences, Inc. and Tupperware Brands Corporation.
Measured PeriodLFVN
NASDAQ Composite
Peer Group
June 30, 2010$100.00
$100.00
$100.00
June 30, 2011$294.12
$132.73
$142.17
June 30, 2012$554.90
$142.01
$111.15
June 30, 2013$454.90
$167.01
$139.34
June 30, 2014$282.35
$219.06
$144.20
June 30, 2015$103.92
$250.68
$105.98
Dividends

We have not declared any dividends on any class of our equity securities since incorporation, and we do not currently anticipate declaring any dividendsdividends. Additionally, the Financing Agreement we entered into in the foreseeable future. Other thanOctober 2013 contains customary covenants that, among other things, restrict our previously announced stock repurchase program, we currently intendability to retain our future earnings, if any, for use in our operations and the expansionpay dividends.
Purchases of Equity Securities
There were no shares of our business.

common stock issued during the three months ended June 30, 2015, due to the exercise of warrants.

We did not purchase any shares of our common stock during the quarter ended June 30, 2015.
During the three months ended June 30, 2015, we withheld 0.1 million shares to satisfy tax withholding obligations in connection with the partial vesting of restricted stock awards.
Recent Sale of Unregistered Securities
During the three months ended June 30, 2015, we did not issue any securities that were not registered under the Securities Act of 1933, as amended.
Equity Compensation Plan Information
This information is incorporated by references to Item 12 of this report.
ITEM 6 — SELECTED FINANCIAL DATA

Under SEC rules

The following table summarizes certain historical financial information at the dates and regulations, becausefor the aggregate worldwide market valueperiods indicated prepared in accordance with GAAP. The consolidated statement of our common stock held by non-affiliates was more than $75 million, but less than $700 million, asoperations data for each of December 30, 2011, the last business day of our most recently completed second fiscal quarter, we are considered to be an “accelerated filer.” We were considered to be a “smaller reporting company” when we determined our filing status for purposes of our annual report on Form 10-K for our fiscal yearyears ended June 30, 2011. SEC rules2015, 2014 and regulations provide that a smaller reporting company transitioning to2013, and the larger reporting system,consolidated balance sheet data as we are doingof June 30, 2015, and 2014, have been derived from our consolidated financial statements audited by EKS&H LLLP, an independent registered public accounting firm, included elsewhere in this year, may finish reporting as a smaller reporting companyAnnual Report on Form 10-K. The consolidated statement of operations data for the resteach of the fiscal year, includingyears ended June 30, 2012 and 2011 and the consolidated balance sheet data as of June 30, 2013, 2012 and 2011 have been derived from our financial statements not included herein. The selected consolidated financial data should be read in its annual reportconjunction with “Management's Discussion and Analysis of Financial Condition and Results of Operations” and the consolidated financial statements and notes thereto, which are included elsewhere in this Annual Report on Form 10-K, and is not required to satisfy the larger reporting company disclosure requirements until the first quarterly report for the new fiscal year following the determination date. Accordingly, we10-K. Our historical results are not requirednecessarily indicative of operating results to providebe expected in the information required by this item in this report.

-32-

future.


- 30-



 Years Ended June 30,
 2015 2014 2013 2012 2011
(In thousands, except per share data)         
Statement of Operations Data:         
Revenue, net$190,336
 $213,968
 $208,178
 $126,183
 $38,919
Cost of sales28,010
 33,194
 31,845
 18,052
 5,917
Product recall costs
 
 4,798
 
 
          Gross profit162,326
 180,774
 171,535
 108,131
 33,002
Operating expenses:
        
           Commission and incentives91,074
 104,525
 101,737
 57,955
 17,132
           Selling, general and administrative57,353
 56,801
 57,730
 28,719
 12,168
                    Total operating expenses148,427
 161,326
 159,467
 86,674
 29,300
Operating income (loss)13,899
 19,448
 12,068
 21,457
 3,702
Other expense, net:         
         Interest expense(3,087) (3,177) (3) (8) (5,993)
        Other income (expense), net(159) 384
 (912) (36) 45
        Change in fair value of derivative liabilities
 
 
 (6,741) (48,454)
        Total other expense, net(3,246) (2,793) (915) (6,785) (54,402)
Income (loss) before income taxes10,653
 16,655
 11,153
 14,672
 (50,700)
         Income tax expense(3,666) (5,272) (3,545) (2,203) (92)
Net income (loss)$6,987
 $11,383
 $7,608
 $12,469
 $(50,792)
Net income (loss) per share:         
Basic$0.07
 $0.11
 $0.07
 $0.12
 $(0.69)
Diluted$0.07
 $0.10
 $0.06
 $0.11
 $(0.69)
Weighed average shares outstanding:         
Basic97,293
 105,791
 112,276
 102,696
 73,173
Diluted99,052
 111,599
 122,888
 118,331
 73,173
 As of June 30,
 2015 2014 2013 2012 2011
(In thousands)         
Balance Sheet Data:         
Cash and cash equivalents$13,905
 $20,387
 $26,299
 $24,648
 $6,721
Working capital4,615
 17,271
 25,375
 22,800
 (3,105)
Total assets40,879
 53,999
 55,484
 44,528
 12,499
Current liabilities25,860
 22,702
 20,566
 16,028
 13,380
Derivative liabilities
 
 
 
 19,905
Long-term debt, net of unamortized discount9,631
 25,073
 
 
 
Total liabilities37,554
 50,009
 21,539
 16,245
 33,307
Total stockholders equity (deficit)3,325
 3,990
 33,945
 28,283
 (20,808)

- 31-





ITEM 7 — MANAGEMENT’S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS

You should read the following discussion and analysis in connection with our financial statements and related notes beginning on page F-1 following Part III of this report.

Overview

We are a company dedicated to helping people achieve their health, wellness and financial independence goals. We provide quality, scientifically validated products and a financially rewarding network marketing business opportunity to customers and independent distributors who seek a healthy lifestyle and financial freedom. We sell our products in the United States, Japan, Australia and Mexico through a network of independent distributors, and to preferred and retail customers. We also sell our products directly to consumers located in Canada for personal consumption.

We engage in the identification, research, development manufacture and distribution of advanced nutraceutical dietary supplements including our flagship product, Protandim®, the Nrf2 Synergizer®and our anti-aging skin care product, LifeVantage TrueScience®.products. We currently focussell our ongoing internal research effortsproducts to independent distributors and preferred customers in two geographic regions: Americas and Asia/Pacific.

Our revenue depends on oxidative stress solutions, particularly the activationnumber and productivity of Nuclear factor (erythroid-derived 2)-like 2, also known as Nrf2, asour independent distributors and the number of our preferred customers. When we are successful in attracting and maintaining independent distributors and preferred customers, it relates to health-related disorders.is largely because of:
Our scientifically-validated products, including Protandim®, LifeVantage TrueScience®, Canine Health® and Axio®;

Our compensation plan and other sales initiatives; and

Our goal to deliver superior customer service.
As a result, it is vital to our success that we leverage our product development resources to develop and introduce innovative products and provide opportunities for our independent distributors to sell these products in a variety of markets.
We have begun selling our products in and attracting new independent distributors and preferred customers in several new markets since the beginning of our direct selling activities in 2009, including Japan, Australia, Canada, Mexico, Hong Kong, Thailand and, on a limited basis, the Philippines. Entering a new market requires a considerable amount of time, resources and continued support. If we are unable to properly support an existing or new market, our revenue growth will be negatively impacted.
Our Products

Our products are Protandim® and, the LifeVantage TrueScience® skin care regimen, Axio®. Protandim, and Canine Health® is. Protandim® contains a proprietary blend of ingredients thatand has been shown to combat oxidative stress by increasing the body’s natural antioxidant protection at the genetic level, inducing the production of naturally-occurring protective antioxidant enzymes including superoxide dismutase, catalase, and glutathione synthase. Our LifeVantage TrueScience® skin care regimen includes TrueScience® Ultra Gentle Facial Cleanser, TrueScience® Perfecting Lotion, TrueScience® Eye Corrector Serum, and our enhanced TrueScience® Anti-Aging Cream. Axio® is our science-based anti-aging skin care product, which incorporates some of the ingredients found in our Protandimenergy drink mix formulated to promote alertness and support mental performance. Canine Health® is a supplement specially formulated to combat oxidative stress in dogs through Nrf2 activation. The following table shows revenues by major product with other proprietary ingredients.line for the years ended June 30, 2015, 2014 and 2013.

 For the years ended June 30,
 2015 2014 2013
Protandim®
$120,967
 63.6% $142,935
 66.8% $138,996
 66.8%
LifeVantage TrueScience® skin care regimen
38,287
 20.1% 46,474
 21.7% 42,229
 20.3%
Other31,082
 16.3% 24,559
 11.5% 26,953
 12.9%
Total$190,336
 100.0% $213,968
 100.0% $208,178
 100.0%
We sell ourThe Company's revenues are largely attributed to two products lines, Protandim® and the LifeVantage TrueScience®skin care regimen, which each accounted for more than 10% of total revenues for each of the years ended June 30, 2015, 2014 and 2013. On a combined basis, these products represent approximately 83.7%, 88.5% and 87.1% of our worldwide gross revenues for the years ended June 30, 2015, 2014 and 2013, respectively.

- 32-



We currently have additional products in development. Any delays or difficulties in introducing compelling products or attractive initiatives or tools into our markets may have a negative impact on our revenue and our ability to attract new independent distributors and preferred customers.
Customers
Because we utilize a direct selling model for the distribution of our products, the success and growth of our business is primarily based on the effectiveness of our independent distributors in selling our products and on our ability to attract new and retain existing independent distributors. Changes in our product sales are typically the result of variations in product sales volume relating to fluctuations in the number of active independent distributors and preferred customers purchasing our products. The number of active independent distributors and preferred customers is, therefore, used by management as a key non-financial measure.
The following tables summarize the changes in our active customer base by geographic region. These numbers have been rounded to the nearest thousand as of the dates indicated. For purposes of this report, we only count as active customers those independent distributors and preferred customers who have purchased from us at any time during the most recent three-month period, either for personal use or for resale. We believe that the decrease in overall preferred customers is a result of a majority of our efforts being focused on attracting independent distributors who both consume our products and seek out others who will also purchase and consume our products.

Active Independent Distributors By Region




As of June 30, 2015 As of June 30, 2014 Change from Prior Year Percent Change
Americas44,000
 67.7% 44,000
 64.7% 
  %
Asia/Pacific21,000
 32.3% 24,000
 35.3% (3,000) (12.5)%

65,000
 100.0% 68,000
 100.0% (3,000) (4.4)%

Active Preferred Customers By Region




As of June 30, 2015 As of June 30, 2014 Change from Prior Year Percent Change
Americas94,000
 81.7% 107,000
 83.6% (13,000) (12.1)%
Asia/Pacific21,000
 18.3% 21,000
 16.4% 
  %

115,000
 100.0% 128,000
 100.0% (13,000) (10.2)%
Income Statement Presentation
We report revenue in two geographic regions and we translate revenue from each market's local currency into U.S. dollars using weighted-average exchange rates. Revenue consists primarily of product sales, fee revenues, and shipping and handling fees net of applicable sales discounts. Revenue is recognized upon the passage of title and risk of loss to customers. Also reflected in revenue is a provision for product returns and allowances, which is estimated based on our historical experience. The following table sets forth net revenue information by region for the periods indicated. The following table should be reviewed in connection with the tables presented under "Results of Operations" (in thousands):
 For the years ended June 30,
 2015 2014 2013
Americas$138,118
 72.6% $141,227
 66.0% $133,046
 63.9%
Asia/Pacific52,218
 27.4% 72,741
 34.0% 75,132
 36.1%
Total$190,336
 100% $213,968
 100% $208,178
 100%
Cost of sales primarily consists of costs of products purchased from and manufactured by third-party vendors, costs of adjustments to inventory carrying value, and costs of sales materials which we sell to our sales force, as well as freight, duties and taxes that are associated with the import and export of our products. As our international sales increase as a percentage of total revenue, cost of sales are increasingly affected by additional duties, freight, and other factors, such as changes in currency exchange rates.
Commissions and incentives expenses are our most significant expenses and are classified as operating expenses. Commissions and incentives expenses include sales commissions paid to our independent distributors, special incentives, costs

- 33-



for incentive trips and other rewards. Commissions and incentives expenses do not include any amounts we pay to our independent distributors for personal purchases. Commissions paid to independent distributors on personal purchases are considered a sales discount and are reported as a reduction to our net revenue. Our global sales compensation plan, which we employ in all our markets, is an important factor in our ability to attract and retain our independent distributors. Under our global sales compensation plan, independent distributors can earn commissions for product sales to their preferred customers as well as the product sales made through the sales network they have developed and trained. We do not pay commissions on sales materials, which are sold to our independent distributors. Commissions and incentives expenses, as a percentage of revenue, may increase in connection with limited-time offers due to growth in the number of independent distributors qualifying for increased sales compensation and promotional incentives. From time to time, we make modifications and enhancements to our global sales compensation plan in an effort to help motivate our sales force and develop leadership characteristics, which can have an impact on commissions and incentives expenses.
Selling, general and administrative expenses include wages and benefits, marketing and event costs, professional fees, rents and utilities, depreciation and amortization, research and development, travel costs, and other operating expenses. Wages and benefits represent the largest component of selling, general and administrative expenses. Marketing and event costs include costs of distributor conventions and events held in various markets worldwide, which we expense in the period in which they are incurred. Marketing and event costs also include expenses associated with our sponsorship of the Major League Soccer team, Real Salt Lake.
Sales to customers outside the United States are transacted in the respective local currencies and are translated to U.S. dollars at weighted-average currency exchange rates for each monthly accounting period to which they relate. Consequently, our net sales and earnings are affected by changes in currency exchange rates. In general, sales and gross profit are affected positively by a weakening U.S. dollar and negatively by a strengthening U.S. dollar. Currency fluctuations, however, have the opposite effect on our commissions paid to independent distributors and toselling, and general and administrative expenses. In our preferred and retail customers.

To date,revenue discussions that follow, we have focused our research effortsapproximate the impact of currency fluctuations on investigating various aspects and consequences ofrevenue by translating current year revenue at the imbalance of oxidants and antioxidants, an abnormality, which is a central underlying featureaverage exchange rates in many disorders. We intend to continue our research, development, and documentation ofeffect during the efficacy of our Protandim® formula to provide credibility to the market. We also anticipate undertaking research, development, testing, licensing and acquisition efforts to be able to introduce additional products in the future, although we may not be successful in this endeavor.

comparable prior year periods.

Results of Operations

We commenced sales of our Protandim® product in February 2005 and our LifeVantage TrueScience® product in June 2009. For the fiscal years ended June 30, 20122015, 2014, and 2011,2013, we generated net revenues of $126,182,848$190.3 million, $214.0 million and $38,919,223,$208.2 million, respectively, recognized operating profit of $21,456,384$13.9 million, $19.4 million and $3,702,204,$12.1 million, respectively, and incurredrecognized net income (loss) of $12,469,077$7.0 million, $11.4 million and $(50,791,750)$7.6 million, respectively.

Our expenditures consist primarily of independent distributor commissions, operating expenses, payroll and professional fees, customer service, research and development and product manufacturing for the marketing and sale of Protandim®.

-33-


The following table presents certain consolidated earnings data as a percentage of net sales:

   For the years ended, 
   June 30, 2012  June 30, 2011 

Sales, net

   100  100

Cost of sales

   14.3    15.2  
  

 

 

  

 

 

 

Gross profit

   85.7    84.8  

Operating expenses:

   

Sales and marketing

   54.2    54.1  

General and administrative

   13.0    19.3  

Research and development

   1.1    1.3  

Depreciation and amortization

   0.4    0.6  
  

 

 

  

 

 

 

Total operating expenses

   68.7    75.3  
  

 

 

  

 

 

 

Operating income

   17.0    9.5  

Other income and (expense):

   

Interest expense, net

   0.0    (15.3

Change in fair value of derivative liabilities

   (5.4  (124.5
  

 

 

  

 

 

 

Total other (expense)

   (5.4  (139.8
  

 

 

  

 

 

 

Net income (loss) before income taxes

   11.6    (130.3

Income tax expense

   (1.7  (0.2
  

 

 

  

 

 

 

Net income (loss)

   9.9  (130.5)% 
  

 

 

  

 

 

 

revenue:

 For the years ended,
 June 30, 2015 June 30, 2014 June 30, 2013
Revenue, net100.0 % 100.0 % 100.0 %
Cost of sales14.7
 15.5
 15.3
Product recall costs
 
 2.3
Gross profit85.3
 84.5
 82.4
Operating expenses:     
Commissions and incentives47.8
 48.9
 48.9
Selling, general and administrative30.1
 26.5
 27.7
Total operating expenses77.9
 75.4
 76.6
Operating income7.4
 9.1
 5.8
Other income (expense):     
Interest expense(1.6) (1.5) 
Other income (expense), net(0.1) 0.2
 (0.4)
Total other income (expense)(1.7) (1.3) (0.4)
Income before income taxes5.7
 7.8
 5.4
Income tax expense(1.9) (2.5) (1.7)
Net income3.8 % 5.3 % 3.7 %
Comparison of Fiscal Years Ended June 30, 20122015 and 20112014

Sales.Revenue, net.We generated net revenue of $190.3 million and $214.0 million during the years ended June 30, 2015 and 2014, respectively. This included decreases in both the Americas region and the Asia/Pacific region. Foreign currency

- 34-



fluctuations negatively impacted our net revenue $6.0 million or 2.8%, which is related primarily to our Asia/Pacific region. The overall decrease in sales of $126,182,848$23.6 million in fiscal 2015 was primarily due to a decrease of $20.5 million in sales in the Asia/Pacific region caused by both the negative foreign currency impact on sales and distractions in the distributor force in Japan.
Americas. The following table sets forth revenue for the years ended June 30, 2015 and 2014 for the Americas region (in thousands):
 For the years ended June 30,  
 2015 2014 % change
United States$132,831
 $136,758
 (2.9)%
Other5,287
 4,469
 18.3 %
Americas Total$138,118
 $141,227
 (2.2)%
Revenue in the Americas region for the year ended June 30, 2015 decreased $3.1 million or 2.2%. The decrease in revenue during the year ended June 30, 2012 and $38,919,223 during the year ended June 30, 2011 primarily from the sale of our Protandim® and LifeVantage TrueScience® products. The increase in sales of $87,263,625 was primarily2015 is due to significant growtha decrease in the number of independent distributors andactive preferred customers of 12.1% and included an increase inlower volume of product sales in the Americasregion as compared to the prior year same period, offset partially by additional product purchases associated with the launch of $54,645,186Axio®, our new energy drink product.
Asia/Pacific. The following table sets forth revenue for the years ended June 30, 2015 and sales2014 for the Asia/Pacific region and its principal markets (in thousands):
 For the years ended June 30,  
 2015 2014 % change
Japan$41,428
 $61,872
 (33.0)%
Hong Kong5,963
 7,347
 (18.8)%
Other4,827
 3,522
 37.1 %
Asia/Pacific Total$52,218
 $72,741
 (28.2)%
Revenue in Japan of $32,618,439. We expect the growth in sales to continue in our fiscal 2013 year as we continue to add new independent distributors and preferred customers and expand into additional international markets.

Gross Margin.Cost of sales were $18,052,151region for the year ended June 30, 2012,2015 was negatively impacted approximately $5.5 million, or 7.6%, by foreign currency exchange rate fluctuations.

Local currency revenue in Japan decreased 24.4% in fiscal 2015 compared to fiscal 2014. During the year ended June 30, 2015 the Japanese yen weakened against the U.S. dollar, negatively impacting our revenue in this market by $5.3 million or 8.6%. In addition to the negative impact of foreign currency fluctuations, product sales volume decreased in Japan and $5,917,394Hong Kong. The negative impact of foreign currency rate fluctuations and the decrease in product sales was partially offset by an increase in volume of product sales in Australia, Philippines and Thailand.
All of our sales and marketing efforts continue to be directed toward building our network marketing sales. We expect increased revenue in the Americas region as we continue to focus on our growth initiatives, specifically product development and sales and marketing. We expect revenue in Australia, Hong Kong, and the Philippines to remain relatively consistent as we continue to provide similar levels of support as previous periods. Overall, we expect revenues to increase moderately as we continue to focus on strengthening our sales and marketing efforts, product innovation, and expanding our geographic reach.
We continue to face significant challenges in our Japan market, with our biggest challenge being the contraction in revenue. We believe that continued attempts by former distributors, including two previous lead distributors, who terminated their distributorships in June 2014 after being suspended for ongoing violations of our policies and procedures, to recruit our distributors to another network marketing company has continued to be a distraction and negatively impact our business in that market.
While there continues to be uncertainty regarding the full impact these distractions will have on future revenue, we have taken actions to mitigate the impact and we continue to monitor the progress of these actions. We have commenced and continue to take legal action against the company to which some of our former distributor leaders have moved, but anticipate that will take time to complete. In addition, we are working to unify our Japan distributor base, starting with our distributor leaders in the market. We have restructured our Japan field advisory board, with the intended effect to streamline the partnership process and focus leaders on positive in-country distributor activities. In addition to promoting greater leadership and unity in the market, we are focused on creating country-specific marketing tools and materials that we believe will be of significant benefit to our distributors as they build their businesses.

- 35-



Gross Margin. Cost of sales were $28.0 million for the year ended June 30, 2011,2015, and $33.2 million for the year ended June 30, 2014, resulting in a gross margin of $108,130,697,$162.3 million, or 86%85%, and $33,001,829,$180.8 million, or 85%84%, respectively. The increase in gross margin percentage isas a percent of revenues was primarily due to slightly decreased inventory-related expenses and adjustments to our sales return reserve estimate.cost recoveries from insurance of approximately $2.0 million that were received during the first quarter of fiscal year 2015. We expect the gross margin percentage to remainbe in the current84-85% range for the foreseeable future due to relative stability ofbased on our expected inventory costs at present.and manufacturing costs. Economic conditions and changes in the supply of raw materials, new products with differing raw material cost basis, and additional manufacturing process costs could negatively impact our gross margins in the future.

Operating Expenses.Total operating expenses for the year ended June 30, 20122015 were $86,674,313$148.4 million as compared to operating expenses of $29,299,625$161.3 million for the year ended June 30, 2011.2014. Operating expenses consist of salescommissions and marketingincentives expenses and selling, general and administrative research and development, and depreciation and amortization. The majorityexpenses. Operating expenses as a percentage of the increase of $57,374,688 in operating expenses is duerevenue increased to independent distributor commissions on our increased network marketing sales.

Sales and Marketing.Sales and marketing expense77.9% for the year ended June 30, 2012 was $68,397,356 compared2015 from 75.4% for the year ended June 30, 2014. The decrease of $12.9 million in operating expenses is due primarily to $21,060,213decreased commissions and incentives expenses caused by our decreased sales. The increase in operating expenses as a percentage of revenues is due to increased wage and salary expenses associated with changes in the Company's executive team as well as increased costs related to marketing events held during the fiscal year ended June 30, 2015.

Primary factors that may cause our operating expenses to fluctuate in the future include changes in the number of employees, foreign exchange rates, and the impact of our variable compensation programs, which are driven by overall operating results. A fluctuation in our stock price may also impact our share-based compensation expense recorded for liability classified awards.
Commissions and Incentives. Commissions and incentives expenses for the fiscal year ended June 30, 2011 representing an increase2015 were $91.1 million or 47.8% of $47,337,143revenue compared to $104.5 million or 48.9% of revenue for the fiscal year ended June 30, 2014. The decrease in expense of $13.5 million in fiscal year 2012. This increase2015 was due primarily to commissions incurred on increased sales as well as increased event and promotion costs and increased headcount related costs.the overall decrease in sales. We expect salescommissions and marketingincentives expenses to continue to increase relative to increases in sales and to remain relatively stable as a percentage of net sales.sales, with some small fluctuations caused by changes to compensation and incentive programs.

-34-


Selling, General and Administrative.Our Selling, general and administrative expenseexpenses for the year ended June 30, 2012 was $16,396,6312015 were $57.4 million compared to $7,516,106$56.8 million for the fiscal year ended June 30, 2011.2014. The increase of $8,880,525$0.6 million was primarily due to an increaseincreased wage expenses associated with changes in headcount relatedthe executive team and increased research and development costs as well asdue to increased professional fees, stock compensation expenses, insurance and travel. spending on product innovation.
We expect ourselling, general and administrative expenses, as a percent of revenue, to increase as we experience continued growth.

Researcha result of our strategic initiatives around strengthening our sales and Development.Our researchmarketing efforts, product innovation, and development expense for the year ended June 30, 2012 was $1,359,055 compared to $508,603 for the year ended June 30, 2011. The increase of $850,452 was due primarily to increased headcount related costs.expanding our geographic reach.

Other Income (Expense). We expect research and development expenses to increase as we continue to develop our products.

Depreciation and Amortization.Depreciation and amortization for the year ended June 30, 2012 was $521,271 compared to $214,703 for the year ended June 30, 2011. The increase of $306,568 primarily relates to fixed asset acquisitions during the year ended June 30, 2012.

Net Other Expense.We recognized net other expense for the year ended June 30, 20122015 of $6,784,759$3.2 million as compared to $54,401,954$2.8 million for the year ended June 30, 2011.2014. Other expense decreased by $47,617,195,for the year ended June 30, 2015 consisted primarily due to a decreaseof interest expense of $3.1 million and the impact of changes in fair value expense related to derivative liabilities as the instruments were either exercised or the derivative provision was removed.foreign currency exchange rates. As of June 30, 2012,2015, we havehad no derivative liability instruments outstanding and do not expect to recognize expense or income relating to derivative liability in future periods.

The following table sets forth interest expense for the years ended June 30, 2015 and 2014 (in thousands):
 For the years ended June 30,
 2015 2014
Contractual interest expense:   
2013 Term Loan$2,633
 $2,732
Amortization of deferred financing fees:   
2013 Term Loan255
 158
Amortization of debt discount:   
2013 Term Loan198
 123
Other1
 164
Total interest expense$3,087
 $3,177
Income Tax Expense. Our income tax expense for the year ended June 30, 20122015 was $2,202,548$3.7 million as compared to income tax expense of $92,000$5.3 million for the year ended June 30, 2011. The increase in tax expense is due to2014. Our provision for income taxes for the increase in taxable income and is partially offset by the release of our valuation allowance against deferred tax assets in the second quarter of the fiscal year ended June 30, 2012.2015 consisted primarily of federal, state, and foreign tax on anticipated fiscal 2015 income which was partially offset by tax benefits

- 36-



related to research and development credits and a deduction for domestic production activities. We expect our income tax expense and effective tax rate to increase as our taxable income increases and our effective rate approaches normal statutory rates in future periods.

Net Income (Loss).OurIncome. As a result of the foregoing factors, net income for the year ended June 30, 2012 was $12,469,077 as2015 decreased to $7.0 million compared to the net loss of $50,791,750$11.4 million for the year ended June 30, 2011.2014.
Comparison of Fiscal Years Ended June 30, 2014 and 2013
Revenue. We generated net revenue of $214.0 million and $208.2 million during the years ended June 30, 2014 and 2013, respectively. This representsincluded an increase in net income of $63,260,827revenue in the Americas region and a slight decline in net revenue in the Asia/Pacific region. Foreign currency fluctuations negatively impacted our net revenue $10.4 million or 5.0%, which is comprisedrelated primarily to our Asia/Pacific region. The increase in sales of $5.8 million in fiscal 2014 was primarily due to an increase of 2.3% in active independent distributors in the Americas as well as the successful introduction of a full line of anti-aging skin care products under our LifeVantage TrueScience® brand in fiscal 2014.
Americas. The following table sets forth revenue for the years ended June 30, 2014 and 2013 for the Americas region (in thousands):

For the years ended June 30, 

2014 2013 % change
United States$136,758
 $131,508
 4.0%
Other4,469
 1,538
 190.6%
Americas Total$141,227
 $133,046
 6.1%
Revenue in the Americas region for the year ended June 30, 2014 increased $8.2 million or 6.1% . The increase in revenue during the year ended June 30, 2014 is due to an increased number of active independent distributors and higher volume of product sales in the region as compared to the prior year same period, including additional product sales associated with the launch of our full line of anti-aging skin care products under our LifeVantage TrueScience® brand.
Asia/Pacific. The following table sets forth revenue for the years ended June 30, 2014 and 2013 for the Asia/Pacific region and its principal markets (in thousands):
 For the years ended June 30,  
 2014 2013 % change
Japan$61,872
 $69,491
 (11.0)%
Hong Kong7,347
 2,478
 100.0 %
Other3,522
 3,163
 11.3 %
Asia/Pacific Total$72,741
 $75,132
 (3.2)%
Revenue in the region for the year ended June 30, 2014 was negatively impacted approximately $10.1 million, or 13.5%, by foreign currency exchange rate fluctuations.
Local currency revenue in Japan increased 3.2% in fiscal 2014 compared to fiscal 2013. During the year ended June 30, 2014 the Japanese yen weakened against the U.S. dollar, negatively impacted our revenue in this market by $9.8 million or 14.1%. The negative impact of foreign currency rate fluctuations was partially offset by an increase in volume of product sales in Japan and Hong Kong. Effective April 1, 2014 we implemented a price increase in our Japan market of 20% to offset the yen devaluation.
Gross Margin. Cost of sales were $33.2 million for the year ended June 30, 2014, and $36.6 million for the year ended June 30, 2013, resulting in a gross margin of $180.8 million, or 84%, and $171.5 million, or 82%, respectively. The increase in gross margin was primarily caused by our voluntary recall which occurred in the prior fiscal year, December 2012.
Operating Expenses. Total operating incomeexpenses for the year ended June 30, 2014 were $161.3 million as compared to operating expenses of $17,754,180,$159.5 million for the year ended June 30, 2013. Operating expenses consist of commission and incentives expenses and selling, general and administrative expenses. The increase of $1.9 million in operating expenses was due to an increase in commissions and incentives expenses on our increased sales and partially offset by a reduction in selling, general and administrative expenses.

- 37-



Commissions and Incentives. Commissions and incentives expenses for the year ended June 30, 2014 were $104.5 million or 48.9% compared to $101.7 million or 48.9% for the fiscal year ended June 30, 2013. The increase in expense of $2.8 million in fiscal year 2014 was due primarily to commissions incurred on increased sales.
Selling, General and Administrative. Our selling, general and administrative expenses for the year ended June 30, 2014 were $56.8 million compared to $57.7 million for the fiscal year ended June 30, 2013. The decrease of $0.9 million was primarily due to a decrease in other expenseresearch and development costs that resulted from a reduction in salaries and benefits related to the retirement of $47,617,195our former Chief Science Officer, Dr. McCord, and partially offset by increased spending on product innovation and an increase in salaries and wages as a result of hiring additional key employees.
Other Income (Expense). We recognized net other expense for the year ended June 30, 2014 of $2.8 million as compared to $0.9 million for the year ended June 30, 2013. Other expense for the year ended June 30, 2014 consisted primarily of interest expense of $3.2 million offset by income related to a government-sponsored business development incentive and impacts of changes in foreign currency exchange rates.
Income Tax Expense. Our income tax expense for the year ended June 30, 2014 was $5.3 million as compared to income tax expense of $2,110,548.$3.5 million for the year ended June 30, 2013. The decrease in tax expense is primarily due to the decrease in income before taxes for the fiscal year ended June 30, 2014 as compared to the fiscal year ended June 30, 2013. The effective tax rates remained consistent at 31.50% and 31.70% for the fiscal years ended June 30, 2014 and 2013, respectively.

Net Income. As a result of the foregoing factors, net income decreased to $11.4 million for the year ended June 30, 2014 compared to $7.6 million in for the year ended June 30, 2013.
Liquidity and Capital Resources

Liquidity
Our primary liquidity and capital resource requirements are to service our debt and finance the cost of our planned salesoperating expenses and marketing efforts, the manufactureworking capital (principally inventory purchases), as well as capital expenditures and sale of our Protandim® and LifeVantage TrueScience® products and to pay our general and administrative expenses. Our primary sources of liquidity arestock repurchases. We have generally relied on cash flow from the sales of our products.

operations to fund operating activities and we have, at times, incurred long-term debt in order to fund stock repurchases and strategic transactions.

At June 30, 2012,2015, our cash and cash equivalents were $24,647,585.$13.9 million. This represented an increasea decrease of $18,276,611$6.5 million from the $6,370,974$20.4 million in cash and cash equivalents and marketable securities as of June 30, 2011.2014. During the fiscal year ended June 30, 2012,2015, our net cash provided by operating activities was $19,388,948$13.2 million as compared to net cash provided by operating activities of $4,680,925$12.1 million during the fiscal year ended June 30, 2011.2014. The increase in cash provided by operating activities during the fiscal year ended June 30, 20122015 is primarily due to an increaseincreased collection of receivables and a decrease in revenues and operating incomeprepayments made for expenses during the fiscal year ended June 30, 2012.

2015, partially offset by the decrease in net income for fiscal year 2015 compared to fiscal year 2014.

During the fiscal year ended June 30, 2012,2015, our net cash used in investing activities was $1,896,272,$1.2 million, primarily due to purchases of fixed assets to support our continued growth.capital expenditures. During the fiscal year ended June 30, 2011,2014, our net cash used in investing activities was $88,967,$2.2 million, also primarily due to the purchases of equipment and intangible assets offset by the redemption of available-for-sale marketable securities.

-35-


capital expenditures.

Cash provided byused in financing activities during the fiscal year ended June 30, 20122015 was $745,449,$18.5 million, compared to cash provided by financing activities of $169,246$15.8 million during the fiscal year ended June 30, 2011.2014. Cash provided byused in financing activities during the fiscal year ended June 30, 2012 was due to exercises of options2015 included principal payments on the Term Loan entered into in October 2013 totaling $9.2 million and warrants offset by our repurchaserepurchases of shares of our outstanding common stock and the repayment of our line of credit.totaling $9.9 million. Cash provided byused in financing activities during the fiscal year ended June 30, 20112014 was primarily due to the exerciserepurchases of options and warrants.

shares of our common stock of $46.2 million that was partially offset by proceeds from the Term Loan of $45.8 million. Principal payments of $16.2 million were made towards the Term Loan during the fiscal year ended June 30, 2014.

At June 30, 2012,2015 and 2014, the total amount of our foreign subsidiary cash was $5.2 million and $2.8 million, respectively. For earnings considered to be indefinitely reinvested, we have not accrued taxes. If we were to remit the cash and cash equivalents from our foreign subsidiaries to our U.S. consolidated group for the purpose of repatriation of undistributed earnings, we would need to accrue and pay taxes. As of June 30, 2015, our U.S. consolidated group had approximately $0.1 million of permanently reinvested unremitted earnings from our subsidiaries, and if these earnings were remitted, the impact of any tax consequences on our overall liquidity position would not be material. We do not have any plans to repatriate these unremitted earnings to our parent; therefore, we do not have any liquidity concerns relating to these unremitted earnings and related cash and cash equivalents.
At June 30, 2015, we had working capital (current assets minus current liabilities) of $22,800,185$4.6 million compared to negative working capital of $(3,105,045)$17.3 million at June 30, 2011.2014. The increasedecrease in working capital was due primarily to increasesdecreases in cash, inventoryincome tax

- 38-



receivable, and deferred tax assetsprepaid expenses as well as an increase in short term debt. We believe that our cash and the elimination of short-term derivative liabilities. These increases were partially offset by increases in accrued expenses including commissions payable. Based oncash equivalents balances and our forecastedongoing cash flow for fiscal 2013 we expect cash on handfrom operations will be sufficient to fundsatisfy our cash requirements for at least the next 12 months. The majority of our historical expenses have been variable in nature and, as such, a potential reduction in the level of revenue would reduce our cash flow needs. In the event that our current cash balances and future cash flow from operations through June 30,are not sufficient to meet our obligations or strategic needs, we would consider raising additional funds, which may not be available on terms that are acceptable to us, or at all. Our credit facility, however, contains covenants that restrict our ability to raise additional funds in the debt or equity markets and repurchase our equity securities without prior approval from the lender. Additionally, we would consider realigning our strategic plans including a reduction in capital spending.
Capital Resources
On October 18, 2013, we entered into a Financing Agreement providing for a term loan facility in an aggregate principal amount of $47 million (the “Term Loan”) and a delayed draw term loan facility in an aggregate principal amount not to exceed $20 million (the “Delayed Draw Term Loan”). The Delayed Draw Term Loan was available for borrowing in specified minimum amounts from time to time beginning after the foreseeable future thereafter.

Off-Balance Sheet Arrangements

effective date (as defined in the Financing Agreement) until October 18, 2014 or until the Delayed Draw Term Loan is reduced to zero, if earlier. We did not haveborrow any off-balance sheet arrangementsamounts under the Delayed Draw Term Loan.

On May 1, 2015, we entered into an Amendment No. 1 to Financing Agreement ("Amendment No. 1"). Amendment No. 1 revised the covenants relating to minimum consolidated EBITDA (as defined in the Financing Agreement) for the four consecutive fiscal quarters ending March 31, 2015 and June 30, 2015 from $20.6 million and $21.3 million, respectively, to $17.0 million for each quarter end. Amendment No. 1 also revised the minimum unrestricted cash and cash equivalents that we are required to hold from $10.0 million to $8.0 million for the reporting periods ended March 31, 2015 and June 30, 2015. In addition, Amendment No. 1 required that we make certain accelerated principal payments on the Term Loan totaling $4.5 million during the fourth quarter of fiscal year 2015.
On August 27, 2015 we entered into an Amendment No. 2 to Financing Agreement ("Amendment No. 2" and collectively, with the Term Loan, the "Credit Facility"). Amendment No. 2 revised the covenants related to minimum consolidated EBITDA (as defined in the amended Financing Agreement) for the four consecutive fiscal quarters ending September 30, 2015, December 31, 2015, March 31, 2016 and June 30, 2016 from $22.2 million, $23.1 million, $24.4 million and $25.6 million, respectively, to $14.5 million, $15.0 million, $17.0 million and $17.5 million, respectively. In addition, Amendment No. 2 requires that we make additional monthly accelerated principal payments on the Term Loan in the amount of $0.5 million commencing on October 15, 2015 and continuing until the Term Loan has been paid in full. Amendment No. 2 also requires that we make additional accelerated payments at the end of each calendar quarter in the amount of all unrestricted cash on hand as of the close of business on the last day of the quarter in excess of $12.5 million.
The Credit Facility contains customary negative covenants that, among other things, restrict us from undertaking specified corporate actions such as creation of liens, incurrence of additional indebtedness, making certain investments with affiliates, changes of control, having excess foreign cash, issuance of equity, repurchasing our equity securities, and making certain restricted payments, including dividends, without prior approval from the lender. At June 30, 2015, we were in compliance with the applicable non-financial and restrictive covenants under the Term Loan. Additionally, management anticipates that in the normal course of operations, we will be in compliance with the non-financial and restrictive covenants during the ensuing year.
The Credit Facility also contains various financial covenants that require us to maintain a certain consolidated EBITDA, certain leverage and fixed charges ratios as well as a minimum level of liquidity. Specifically, after giving effect to Amendment No. 1 and Amendment No. 2, we must:
Have a consolidated EBITDA (as defined in the Financing Agreement) for the four consecutive fiscal quarters ending September 30, 2015, December 31, 2015, March 31, 2016 and June 30, 2016 of $14.5 million, $15.0 million, $17.0 million and $17.5 million, respectively. Our consolidated EBITDA requirement increases over time to $25.6 million for the four consecutive fiscal quarters ending September 30, 2016 and each period of four consecutive fiscal quarters ending each December 31, March 30, June 30, and September 30, thereafter;
Have a total leverage ratio (as defined in the Financing Agreement) of less than 1.78 to 1.00 for the quarter ended June 30, 2012.

2015. Our leverage ratio requirement decreases over time to 1.25 to 1.00 for the quarter ended June 30, 2016, and remains level thereafter;

Have a fixed charge ratio (as defined in the Financing Agreement) of greater than 1.25 to 1.00 for the four consecutive fiscal quarters ending June 30, 2015 and for each of the four consecutive quarters ending thereafter; and

- 39-



For the fiscal quarter ending September 30, 2015 have no less than $7.0 million in unrestricted cash and cash equivalents at any time when the total leverage ratio is greater than 1.25 to 1.00, and for all fiscal quarters ending subsequent to September 30, 2015 have no less than $8.0 million in unrestricted cash and cash equivalents at any time when the total leverage ratio is greater than 1.25 to 1.00.
At June 30, 2015, we were in compliance with all applicable financial covenants including those under the amended Credit Facility. We anticipate that in the absence of a significant increase to our consolidated EBITDA we likely will not meet our consolidated EBITDA covenants for the reporting periods subsequent to June 30, 2016. We will work with our lender to further revise our financial covenants under the Credit Facility as needed. While we expect to be successful in negotiating with our lender to revise the consolidated EBITDA covenant to a level that will be achievable in light of our current business, it is possible that these negotiations will be unsuccessful.
Commitments and Obligations
The following table summarizes our contractual payment obligations and commitments as of June 30, 2015 (in thousands):
 Payments due by period  
Contractual ObligationsTotal 
Less than
1 year
 1-3 years 3-5 years Thereafter
Long-term debt obligations$21,625
 $11,141
 $10,484
 $
 $
Interest on long-term debt obligations1,993
 1,444
 549
 
 
Operating lease obligations
13,835
 2,427
 5,013
 4,003
 2,392
Total$37,453
 $15,011
 $16,046
 $4,003
 $2,392
Off-Balance Sheet Arrangements
At June 30, 2015 and 2014, we had no off-balance sheet arrangements.
Critical Accounting Policies

We prepare our financial statements in conformity with accounting principles generally accepted in the United States of America. As such, we are required to make certain estimates, judgments, and assumptions that we believe are reasonable based upon the information available. These estimates and assumptions affect the reported amounts of assets and liabilities at the date of the financial statements and the reported amounts of revenues and expenses during the periods presented. Actual results could differ from these estimates. Our significant accounting policies are described in Note 2 to our financial statements. Certain of these significant accounting policies require us to make difficult, subjective, or complex judgments or estimates. We consider an accounting estimate to be critical if (1) the accounting estimate requires us to make assumptions about matters that were highly uncertain at the time the accounting estimate was made and (2) changes in the estimate that are reasonably likely to occur from period to period, or use of different estimates that we reasonably could have used in the current period, would have a material impact on our financial condition or results of operations.

There are other items within our financial statements that require estimation, but are not deemed critical as defined above. Changes in estimates used in these and other items could have a material impact on our financial statements. Management has discussed the development and selection of these critical accounting estimates with the audit committee of our board of directors, and the audit committee has reviewed the following disclosures.

disclosures noted below.

Allowances for Product Returns

We record allowances for product returns at the time we ship the product based on estimated return rates. We offerSubject to some exceptions based on local regulations, customers may return unopened product to us within 30 days of purchase for a 30-day, money back unconditional guaranteerefund of the purchase price less shipping and handling. As of June 30, 2015, our shipments of products sold totaling approximately $14.1 million were subject to all customers.our return policy. In addition, we allow terminating distributors to return up to 30% of unopened, unexpired product that they purchased within the prior twelve months, subject to certain consumption limitations. As of June 30, 2012, our shipments of products sold totaling approximately $13,755,361 were subject to the money back guarantee.

months.

We monitor our return estimate on an ongoing basis and revise the allowances to reflect our experience. Our allowance for product returns was $862,602 on$0.1 million at June 30, 2012,2015, compared with $435,135 on$0.6 million at June 30, 2011. For the year ended June 30, 2012 we reduced the amount of our reserve by approximately $300,000 to reflect historical return rates lower than our estimate at the beginning of the year.2014. To date, product expiration dates have not played any role in product returns, and we do not expect they will in the future because it is unlikely that we will ship product with an expiration date earlier than the latest allowable product return date.

-36-


- 40-



Inventory Valuation

We state inventoriesvalue our inventory at the lower of cost or market value on a first-in, first-out basis. From timeAccordingly, we reduce our inventories for the diminution of value resulting from product obsolescence, damage or other issues affecting marketability equal to time, we maintain a reserve forthe difference between the cost of the inventory obsolescence and we base this reserve on assumptions about current and future product demand, inventory whose shelf life has expired, andits estimated market conditions. From time to time, we may be required to make additional reservesvalue. Factors utilized in the event anydetermination of these variables change. estimated market value include (i) current sales data and historical return rates, (ii) estimates of future demand, (iii) competitive pricing pressures, (iv) new production introductions, (v) product expiration dates, and (vi) component and packaging obsolescence.
We have recorded $34,628 in reserves$0.3 million of obsolescence costs for obsolete inventory as of the year ended June 30, 20122015. For the year ended June 30, 2014 we recorded $0.8 million of inventory write-downs primarily related to inventory of marketing materials. As of June 30, 2011 we had recorded $74,943our voluntary recall in reserves for obsolete inventory.

December 2012.

Revenue Recognition

We ship the majority of our product directly to the consumer through network marketing sales via UPS and we receive substantially all payment for these sales in the form of credit card charges. We recognize revenuereceipts. Revenue from direct product sales to customers is recognized upon passage of title and risk of loss to customers when product ships from the fulfillment facility. Sales revenue and estimated returns are recorded when product is shipped.

Derivative Instruments

In the past, in connection with the sale of debt or equity instruments, we sold options or warrants to purchase our common stock. Prior to March, 31, 2012, these options or warrants were classified as derivative liabilities, rather than as equity. Additionally, the debt or equity instruments contained embedded derivative instruments, such as conversion options, which in certain circumstances were required to be bifurcated from the associated host instrument and accounted for separately as a derivative instrument liability.

We estimated fair values of derivative financial instruments using various techniques that are considered to be consistent with the objective measurement of fair values. In selecting the appropriate technique, we considered, among other factors, the nature of the instrument, the market risks that it embodies and the expected means of settlement. For less complex derivative instruments, such as freestanding warrants, we generally used the Black Scholes Merton option valuation technique, adjusted for the effect of dilution, because it embodies all of the requisite assumptions (including trading volatility, estimated terms, and risk free rates) necessary to fair value these instruments. For embedded conversion features we generally used a lattice technique because it contains all the requisite assumptions to value these features. Estimating fair values of derivative financial instruments required the development of significant and subjective estimates that may, and are likely to, change over the duration of the instrument with related changes in internal and external market factors. In addition, option-based techniques are highly volatile and sensitive to changes in the trading market price of our common stock. Since derivative financial instruments are initially and subsequently carried at fair values, our income or loss would reflect the volatility in changes to these estimates and assumptions.

As of June 30, 2012, we have eliminated the balances in both short- and long-term derivative liabilities. With a warrant modification approved in December 2011, and the exercise of certain other warrants in March 2012, we have removed all derivative warrant liabilities from the balance sheet and recognized the final changes in fair value of these warrants in the income statement.

loss.

Stock-Based Compensation

We use the fair value approach to account for stock-based compensation in accordance with current accounting guidance.

We recognize compensation costs for awards with performance conditions when we conclude it is probable that the performance conditions will be achieved. We reassess the probability of vesting at each balance sheet date and adjust compensation costs based on our probability assessment. For awards with market conditions, the cost of the awards is recognized as the requisite service is rendered by the employees, regardless of when, if ever, the market conditions are satisfied.

Research and Development Costs

We expense all of our paymentscosts related to research and development activities.

-37-


Commitments and Obligations

   Payments due by period 

Contractual Obligations

  Total   Less than
1 year
   1-3 years   3-5 years 

Operating Lease Obligations

  $2,878,335    $626,042    $1,672,383    $579,910  

activities as incurred.

Recently Issued Accounting Standards

Refer to “Item 8. Financial Statements and Supplementary Data” and Note 2 to our consolidated financial statements included in Item 15 of this report for discussion regarding the impact of accounting standards that were recently issued but not yet effective, on our consolidated financial statements.

ITEM 7A — QUANTITATIVE AND QUALITATIVE DISCLOSURES ABOUT MARKET RISK
We conduct business in several countries and intend to continue to grow our international operations. Net revenue, operating income, and net income are affected by fluctuations in currency exchange rates and other uncertainties in doing business and selling products in more than one currency.

Under SEC rules In addition, our operations are exposed to risks associated with changes in social, political and economic conditions inherent in international operations, including changes in the laws and policies that govern international investment in countries where we have operations, as well as, to a lesser extent, changes in U.S. laws and regulations asrelating to international trade and investment.

Foreign Currency Risk
During the year ended June 30, 2015, approximately 30% of our net revenue was realized outside of the United States. The local currency of each international subsidiary is generally the functional currency. All revenues and expenses are translated at weighted average exchange rates for the periods reported. Therefore, our reported revenue and earnings will be positively impacted by a smaller reporting company transitioningweakening of the U.S. dollar and will be negatively impacted by a strengthening of the U.S. dollar. Currency fluctuations, however, have the opposite effect on our expenses incurred outside the U.S. Given the large portion of our business derived from Japan, any weakening of the Japanese Yen will negatively impact our reported revenue and profits, whereas a strengthening of the Japanese Yen will positively impact our reported revenue and profits. Because of the uncertainty of exchange rate fluctuations, it is difficult to predict the effect of these fluctuations on our future business, product pricing and results of operations or financial condition. Changes in various currency exchange rates affect the relative prices at which we sell our products. We regularly monitor our foreign currency risks and periodically take measures to reduce the risk of foreign exchange rate fluctuations on our operating results. Additionally, we may seek to reduce our exposure to fluctuations in foreign currency exchange rates through the use of foreign currency exchange contracts. We do not use derivative financial instruments for trading or speculative purposes. At June 30, 2015, we did not have any derivative instruments. A 10% strengthening of the U.S. Dollar compared to all of the foreign currencies in which we transact business would have resulted in a 2.8% decrease of our 2015 fiscal year revenue, in the amount of $5.2 million.

- 41-



Following are the average currency exchange rates of U.S. $1 into local currency for each of our international or foreign markets:
 Year ended June 30, 2015 Year ended June 30, 2014
 1st Quarter 2nd Quarter 3rd Quarter 4th Quarter 1st Quarter 2nd Quarter 3rd Quarter 4th Quarter
                
Japan103.93
 114.47
 119.17
 121.35
 98.93
 100.41
 102.83
 102.15
Australia1.08
 1.17
 1.27
 1.29
 1.09
 1.08
 1.12
 1.07
Hong Kong7.75
 7.76
 7.76
 7.75
 7.76
 7.75
 7.76
 7.75
Mexico13.12
 13.87
 14.95
 15.32
 12.91
 13.02
 13.24
 13.00
Canada1.09
 1.14
 1.24
 1.23
 1.04
 1.05
 1.10
 1.09
Thailand32.17
 32.77
 32.71
 33.29
 31.51
 31.77
 32.72
 32.51
Interest Rate Risks
As of June 30, 2015, we had $21.6 million in variable rate debt issued pursuant to the larger reporting company disclosure requirements,Financing Agreement we are not required to provideentered into in October 2013. Based on the information requiredamount of our variable debt as of June 30, 2015, a hypothetical 100 basis point increase or decrease in interest rates on our variable rate debt would increase or decrease our annual interest expense by this item. See “Item 6. Selected Financial Data,” above.

approximately $0.2 million. This change in market risk exposure was driven by our borrowings in connection with our repurchase of shares of our common stock under the November 2013 Dutch auction tender offer in which we accepted for payment an aggregate of 16.3 million shares of our common stock at an aggregate purchase price of $40.0 million.

ITEM 8 — FINANCIAL STATEMENTS AND SUPPLEMENTARY DATA

The information required by this Item 8 is set forth in the consolidated financial statements included in Item 15 of this report and is incorporated into this Item 8 by reference.

ITEM 9 — CHANGES IN AND DISAGREEMENTS WITH ACCOUNTANTS ON ACCOUNTING AND FINANCIAL DISCLOSURE

None.

ITEM 9A — CONTROLS AND PROCEDURES

Evaluation of Disclosure Controls and Procedures

We conducted an evaluation under the supervision and with the participation of our management, including our Chief Executive Officer and Chief Financial Officer, of the effectiveness of our disclosure controls and procedures as of the end of the period covered by this report. The term disclosure controls and procedures, as defined in Rule 13a-15(e) under the Securities Exchange Act of 1934 (the “Exchange Act”), means controls and other procedures of a company that are designed to ensure that information required to be disclosed by the company in the reports it files or submits under the Exchange Act is recorded, processed, summarized and reported, within the time period specified by the SEC’s rules and forms. Disclosure controls and procedures also include, without limitation, controls and procedures designed to ensure that information required to be disclosed by a company in the reports that it files or submits under the Exchange Act is accumulated and communicated to the company’s management, including its principal executive and principal financial officers, or persons performing similar functions, as appropriate, to allow timely decisions regarding required disclosure. In designing and evaluating the disclosure controls and procedures, our management recognized that any controls and procedures, no matter how well designed and operated, can only provide reasonable assurance of achieving the desired control objectives, and in reaching a reasonable level of assurance, our management necessarily was required to apply its judgment in evaluating the cost-benefit relationship of possible controls and procedures. Based on this evaluation, our Chief Executive Officer and Chief Financial Officer have concluded that our disclosure controls and procedures were effective as of the end of the period covered by this report.

-38-


- 42-



Management’s Report on Internal Control Over Financial Reporting

Our management is responsible for establishing and maintaining adequate internal control over financial reporting as defined under the Exchange Act. Our internal control over financial reporting is designed to provide reasonable assurance regarding the reliability of financial reporting and the preparation of financial statements for external purposes in accordance with generally accepted accounting principles. Our internal control over financial reporting includes those policies and procedures that:

1.pertain to the maintenance of records that in reasonable detail accurately and fairly reflect the transactions and dispositions of our assets;

2.provide reasonable assurance that transactions are recorded as necessary to permit preparation of financial statements in accordance with GAAP, and that our receipts and expenditures are being made only in accordance with the authorization of our management and directors; and

3.provide reasonable assurance regarding prevention or timely detection of unauthorized acquisition, use or disposition of our assets that could have a material effect on the financial statements.

Because of its inherent limitations, internal control over financial reporting may not prevent or detect misstatements. Also, projections of any evaluation of effectiveness to future periods are subject to the risk that controls may become inadequate because of changes in conditions, or that the degree of compliance with the policies or procedures may deteriorate.

Under the supervision and with the participation of our management, including our Chief Executive Officer and Chief Financial Officer, we conducted an evaluation of the effectiveness of our internal control over financial reporting as of June 30, 2012.2015. Such evaluation was based on the framework set forth in the report entitledInternal Control — Integrated Framework (2013 framework) issued by the Committee of Sponsoring Organizations of the Treadway Commission (“COSO”). The COSO framework summarizes each of the components of a company’s internal control system, including (i) the control environment, (ii) risk assessment, (iii) control activities, (iv) information and communication, and (v) monitoring. Based on this evaluation, our management, including our Chief Executive Officer and Chief Financial Officer has concluded that our internal control over financial reporting was effective as of June 30, 2012.2015.

The effectiveness of our internal control over financial reporting as of the end of the period covered by this report has been audited by Ekhardt, Steiner & Hottman PC,EKS&H LLLP, an independent registered public accounting firm, as stated in their report which appears herein.

Changes in Internal Control over Financial Reporting

There was no change in our internal control over financial reporting identified in connection with the evaluation required by Exchange Act Rules 13a-15(d) or 15d-15(d) that occurred during our most recently completed fiscal quarter that has materially affected, or is reasonably likely to materially affect, our internal control over financial reporting.

ITEM 9B — OTHER INFORMATION

None.

-39-


PART III

Certain information required by Part III of this report is omitted from this report pursuant to General Instruction G(3) of Form 10-K because we will file a definitive proxy statement pursuant to Regulation 14A for our 20132015 annual meeting of shareholders (the “Proxy Statement”) not later than 120 days after the end of the fiscal year covered by this report, and the information included in the Proxy Statement that is required by Part III of this report is incorporated herein by reference.

ITEM 10 — DIRECTORS, EXECUTIVE OFFICERS AND CORPORATE GOVERNANCE

Incorporated herein by reference to the information to be set forth in the Proxy Statement.

ITEM 11 — EXECUTIVE COMPENSATION

Incorporated herein by reference to the information to be set forth in the Proxy Statement.

ITEM 12 — SECURITY OWNERSHIP OF CERTAIN BENEFICIAL OWNERS AND MANAGEMENT AND RELATED STOCKHOLDER MATTERS.

Incorporated herein by reference to the information to be set forth in the Proxy Statement.


- 43-



ITEM 13 — CERTAIN RELATIONSHIP AND RELATED TRANSACTIONS, AND DIRECTORS INDEPENDENCE

Incorporated herein by reference to the information to be set forth in the Proxy Statement.

ITEM 14 — PRINCIPAL ACCOUNTING FEES AND SERVICES

Incorporated herein by reference to the information to be set forth in the Proxy Statement.

-40-


PART IV


ITEM 15 — EXHIBITS, FINANCIAL STATEMENT SCHEDULES

The following documents are being filed as part of this report:

Financial Statements

See the information beginning on page F-1 of this report.

Exhibits

See the Exhibit Index following the signature page of this report.

-41-


- 44-



SIGNATURES

Pursuant to the requirements of Section 13 or 15(d) of the Securities Exchange Act of 1934, the registrant duly caused this report to be signed on its behalf by the undersigned, thereunto duly authorized.

LifeVantage Corporation.

a Colorado corporation

By:
LifeVantage Corporation.
a Colorado corporation
 
By:/s/    Douglas C. RobinsonDarren Jensen
Douglas C. RobinsonDarren Jensen
Its:President and Chief Executive Officer
Date:September 10, 20121, 2015

Each person whose individual signature appears below hereby constitutes and appoints Douglas C. Robinson, David S. ColbertDarren Jensen and Rob Cutler, andMark Jaggi, each of them, with full power of substitution and resubstitution and full power to act without the other, as his or her true and lawful attorney-in-fact and agent to act in his or her name, place and stead and to execute in the name and on behalf of each person, individually and in each capacity stated below, and to file any and all amendments to this report, and to file the same, with all exhibits thereto, and other documents in connection therewith, with the Securities and Exchange Commission, granting unto said attorneys-in-fact and agents, and each of them, full power and authority to do and perform each and every act and thing, ratifying and confirming all that said attorneys-in-fact and agents or any of them or their or his substitute or substitutes may lawfully do or cause to be done by virtue thereof.

Pursuant to the requirements of the Securities Exchange Act of 1934, this report has been signed below by the following persons on behalf of the registrant and in the capacities and on the dates indicated.

Signature Date Title

/s/    Douglas C. Robinson        

Douglas C. Robinson

Darren Jensen
 September 10, 20121, 2015 

President and Chief Executive Officer; Director

Officer

(Principal Executive Officer)

Darren Jensen

/s/    David S. Colbert        

David S. Colbert

Mark Jaggi
 September 10, 20121, 2015 

Chief Financial Officer

(Principal Financial Officer and

Principal Accounting Officer)

Mark Jaggi

/s/    Elwood Spedden        

Elwood Spedden

Garry Mauro
 September 10, 20121, 2015 Chairman of the Board
Garry Mauro

/s/    Dave Manovich        

Dave Manovich

Michael A. Beindorff
  September 10, 2012Chairman of the Audit Committee

/s/    Joe M. McCord        

Joe M. McCord

September 10, 20121, 2015 Director
Michael A. Beindorff

��
/s/    David W. Brown        

David W. Brown

Dave Manovich
 September 10, 20121, 2015Director and Vice Chairman of the Board
Dave Manovich
/s/    George E. MetzgerSeptember 1, 2015 Director
George E. Metzger

/s/    C. Mike Lu        

C. Mike Lu

Richard Okumoto
 September 10, 20121, 2015 Director
Richard Okumoto

-42-



- 45-



EXHIBIT INDEX
Signature
Exhibit
No.
 DateDocument Description Title

/s/    Garry Mauro        

Garry Mauro

September 10, 2012Director

/s/    George E. Metzger        

George E. Metzger

September 10, 2012Director

/s/    Michael A. Beindorff        

Michael A. Beindorff

September 10, 2012Director

-43-


EXHIBIT INDEX

Exhibit
No.

Document Description

Filed Herewith or Incorporated by Reference From

    3.1

 
3.1Amended and Restated Articles of Incorporation and Statement of Correction to Amended and Restated Articles of Incorporation Exhibit to 4.1 to Registration Statement on Form S-8 (File No. 333-200363) filed on November 19, 2014.
3.2(a)Amended and Restated BylawsExhibit 3.2 to Form 10-K for the fiscal year ended June 30, 2011, filed on September 28, 2011.

    3.2(a)

 Amended and Restated Bylaws Exhibit to Form 10-K for the fiscal year ended June 30, 2011, filed on September 28, 2011.

3.2(b)

 First Amendment of the Amended and Restated Bylaws Exhibit to 3.1 Form 8-K filed on May 31, 20122012.

4.1

 Form of Warrant issued in connection with November 2009 Financing Exhibit 4.2 to Form 8-K filed on November 18, 2009.

4.2

 Amendment to Debentures and Warrants, dated as of December 11, 2009 Exhibit 4.3 to Form 10-Q for the fiscal quarter ended December 31, 2010 filed on February 16, 2010.

4.3

 Form of Restated Warrant issued pursuant to Amended and Restated Securities Purchase Agreement dated December 11, 2009 Exhibit 4.5 to Form 10-Q for the fiscal quarter ended MarchDecember 31, 20102009 filed on February 16, 2010.

4.4

 Form of Restated Common Stock Purchase Warrant issued on each of December 31, 2009, January 20, 2010, February 4, 2010 and February 26, 2010 Exhibit 4.2 to Form 10-Q for the fiscal quarter ended March 31, 2010 filed on May 14, 2010.

4.5

 Form of LifeVantage Corporation Amendment to Warrant Exhibit (a)(1)(ii) to Schedule TO filed on November 29, 2011.

10.1

 Manufacturing and Supply Agreement dated July 1, 2008 between Cornerstone Research and Development and LifeVantage Corporation Exhibit 10.21 to Form 10-K/A for the fiscal year ended June 30, 2009 filed October 28, 2009.

10.2#

 LifeVantage Distributor Compensation Plan Exhibit 10.14 to Form 10-K for the fiscal year ended June 30, 2010 filed on September 15, 2010.

  10.3#

10.3
 Form of Securities Purchase Agreement entered into in connection with November 2009 Financing Exhibit 10.1 to Form 8-K filed on November 18, 2009.

10.4

 Form of Amended and Restated Securities Purchase Agreement originally dated December 11, 2009 Exhibit 10.3 to Form 10-Q for the fiscal quarter ended December 31, 2009 filed on February 16, 2010.

10.5

 Amended and Restated Securities Purchase Agreement dated December 31, 2009, among LifeVantage Corporation and the purchaser parties thereto Exhibit 10.1 to Form 10-Q for the fiscal quarter ended March 31, 2010 filed on May 14, 2010.

10.6

 Amended and Restated Securities Purchase Agreement dated January 20, 2010, among LifeVantage Corporation and the purchaser parties thereto Exhibit 10.2 to Form 10-Q for the fiscal quarter ended March 31, 2010 filed on May 14, 2010.

10.7

 Amended and Restated Securities Purchase Agreement dated February 4, 2010, among LifeVantage Corporation and the purchaser parties thereto Exhibit 10.3 to Form 10-Q for the fiscal quarter ended March 31, 2010 filed on May 14, 2010.

-44-


Exhibit
No.

 

Document Description

 

Filed Herewith or Incorporated by Reference From

10.8

 Amended and Restated Securities Purchase Agreement dated February 26, 2010, among LifeVantage Corporation and the purchaser parties thereto Exhibit 10.4 to Form 10-Q for the fiscal quarter ended March 31, 2010 filed on May 14, 2010.

- 46-



Exhibit
No.
Document DescriptionFiled Herewith or Incorporated by Reference From
10.9#

 LifeVantage Corporation 2007 Long-Term Incentive Plan Appendix B to Proxy Statement filed on Schedule 14A filed on October 20, 2006.

10.10(a)#

 LifeVantage Corporation 2010 Long-Term Incentive Plan effective as of September 27, 2010 and as amended on January 10, 2012as of August 21, 2014 ExhibitAnnex A to Form 8-KProxy Statement on Schedule A filed on January 17, 2012.November 19, 2014.

10.10(b)#

 Form of Nonstatutory Stock Option Agreement for the LifeVantage Corporation 2010 Long-Term Incentive Plan Exhibit 4.4 to Registration Statement on Form S-8 (File No. 333-175104) filed on June 23, 2011.

10.10(c)#

 Form of Incentive Stock Option Agreement for the LifeVantage Corporation 2010 Long-Term Incentive Plan Exhibit 4.5 to Registration Statement on Form S-8 (File No. 333-175104) filed on June 23, 2011.

10.10(d)#

Form of Stock Unit Agreement for the LifeVantage Corporation 2010 Long-Term Incentive PlanExhibit 4.8 to Registration Statement on Form S-8 (File No. 333-200363) filed on November 19, 2014.
10.11#

 LifeVantage Corporation FY 2014 Annual Incentive Plan effective as of July 1, 2010 Exhibit to Form 10-Q for the fiscal quarter ended September 30, 2010 filed on November 8, 2010.

  10.12#

LifeVantage Corporation Annual Incentive Plan effective as of July 1, 2011

Filed herewith

  10.13(a)#

Scientific Advisory Board Agreement effective as of October 1, 2009 by and between LifeVantage Corporation and Dr. Joe McCordExhibit to Form 10-Q for the fiscal quarter ended December 31, 2009 filed on February 16, 2010.

  10.13(b)#

Amendment of Scientific Advisory Board Agreement dated July 21, 2011 by and between LifeVantage Corporation and Dr. Joe McCordExhibit10.12 to Form 10-K for the fiscal year ended June 30, 20112013 filed on September 28, 2011.12, 2013.

  10.13(c)#

 Employment Agreement dated April 1, 2011 by and between 
10.12#LifeVantage Corporation and Dr. Joe McCordFY 2014 Sales Incentive Plan Exhibit 10.13 to Form 10-K for the fiscal year ended June 30, 20112013 filed on September 28, 2011.12, 2013.

  10.13(d)#

 Amendment to Employment Agreement dated July 1, 2011
10.13#LifeVantage Corporation and Dr. Joe McCordFY2015 Annual Incentive Plan Exhibit 10.13 to Form 10-K for the fiscal year ended June 30, 20112014 filed on September 28, 2011.10, 2014.

  10.14(a)#

 
10.14#LifeVantage Corporation FY2015 Sales Incentive PlanExhibit 10.14 to Form 10-K for the fiscal year ended June 30, 2014 filed on September 10, 2014.
10.15#LifeVantage Corporation Performance Incentive PlanFiled herewith.
10.16#LifeVantage Corporation FY2016 Annual Incentive PlanFiled herewith.
10.17#LifeVantage Corporation FY2016 Sales Incentive PlanFiled herewith.
10.18#LifeVantage Corporation Cash Settled Performance-Based Long Term Incentive PlanExhibit 10.14 to Form 10-K for the fiscal year ended June 30, 2013 filed on September 12, 2013.
10.19#Form of Performance Unit AgreementExhibit 10.15 to Form 10-K for the fiscal year ended June 30, 2013 filed on September 12, 2013.
10.20#Form of Performance Unit Agreement - FY 2016 through FY 2018Filed herewith.
10.21#Amended and Restated Employment Agreement between LifeVantage Corporation and Douglas C. Robinson dated effective March 11, 2011 and effective as of March 15, 201124, 2014 Exhibit 10.2 to Form 10-Q for the fiscal quarter ended March 31, 20112014 filed on May 16, 2011.6, 2014.

- 47-



  10.14(b)#

Exhibit
No.
 Amendment to EmploymentDocument DescriptionFiled Herewith or Incorporated by Reference From
10.22#Separation Agreement dated March 23, 2012 by and General Release between LifeVantage Corporation and Douglas C. Robinson effective February 13, 2015 Exhibit 10.1 to Form 8-K filed on March 27, 2012.February 20, 2015.

  10.14(c)#

 Forms of incentive stock option and nonqualifying stock option agreements with Mr. Douglas Robinson dated March 15, 2011 Exhibit to Form 10-K for the fiscal year ended June 30, 2011 filed on September 28, 2011.

-45-


Exhibit
No.

Document Description

Filed Herewith or Incorporated by Reference From

  10.15#

10.23#
 Employment Agreement by and between LifevantageDarren Jensen and LifeVantage Corporation and David W. Brown, dated May 4, 2011 and effective as of April 1, 201126, 2015 Exhibit 10.1 to Form 8-K filed on May 10, 2011.April 29, 2015.

  10.16#

10.24#
 Employment Agreement by and between Carrie McQueenDavid Colbert and Lifevantage Corporation effective as of May 17,August 1, 2012 Exhibit 10.1 to Form 8-K filed on May 18, 2012August 6, 2012.

  10.17#

10.25#
Separation Agreement and General Release between LifeVantage Corporation and David Colbert effective July 3, 2015Filed herewith.
10.26# Employment Agreement by and between Robert Urban and Lifevantage Corporation effective as of May 29, 2012 Exhibit 10.1 to Form 8-K filed on May 31, 20122012.

  10.18

 
10.27#Employment Agreement by and between Donny Osmond Concerts, Inc.Rob Cutler and LifeVantage Corporation dated September 1, 2011effective March 21, 2012 Exhibit 10.17 to Form 10-K for the fiscal year ended June 30, 2013 filed on September 12, 2013.
10.28#Separation Agreement and General Release between LifeVantage Corporation and Rob Cutler effective May 8, 2015Filed herewith.
10.29Lease dated September 22, 2011 between Sandy Park I L.L.C. and LifeVantage CorporationExhibit 10.3 to Form 10-Q for the fiscal quarter ended September 30, 2011 filed on November 14, 2011.

  10.19

 
10.30
Lease dated September 22, 201120, 2012 between Sandy Park III L.L.C. and LifeVantage Corporation.Corporation

 Exhibit 10.1 to Form 10-Q for the fiscal quarter ended September 30, 20112012 filed on November 14, 2011.8, 2012.
10.31First Amendment to Lease entered into as of March 24, 2014 between Sandy Park II L.L.C. and LifeVantage CorporationExhibit 10.3 to Form 10-Q for the fiscal quarter ended March 31, 2014 filed on May 6, 2014.
10.32*Commercial Supply Agreement dated January 31, 2014 between LifeVantage Corporation and Deseret Laboratories, Inc.Exhibit 10.1 to Form 10-Q for the fiscal quarter ended March 31, 2014 filed on May 6, 2014.
10.33*Software Service Agreement with JIA, Inc. dated September 28, 2012Exhibit 1.01 to Form 10-Q/A for the fiscal quarter ended March 31, 2013 filed on May 24, 2013.
10.34*Software License Agreement with JIA, Inc. dated September 28, 2012Exhibit 10.2 to Form 10-Q/A for the fiscal quarter ended March 31, 2013 filed on May 24, 2013.
10.35**Service Agreement entered into as of June 1, 2014 between IntegraCore, LLC and LifeVantageExhibit 10.29 to Form 10-K for the fiscal year ended June 30, 2014 filed on September 10, 2014.
10.36**Commercial Supply Agreement entered into as of May 30, 2014 between LifeVantage Corporation and Wasatch Product DevelopmentExhibit 10.30 to Form 10-K for the fiscal year ended June 30, 2014 filed on September 10, 2014.

- 48-



Exhibit
No.
Document DescriptionFiled Herewith or Incorporated by Reference From
10.37#Financing Agreement, dated October 18, 2013, by and among LifeVantage Corporation, the Guarantors and Lenders party thereto and TCW Special Situations, LLC as Collateral Agent and Administrative AgentExhibit (b) to the Schedule TO-I/A filed on October 18, 2013.
10.38#Amendment No. 1 to Financing Agreement, dated May 1, 2015, by and between LifeVantage Corporation, the Guarantors and lenders party thereto and TCW Special Situations, LLC as Collateral Agent and Administrative AgentExhibit 10.1 to Form 10-Q for the quarter ended March 31, 2015 filed on May 6, 2015.
10.39#
Amendment No. 2 to Financing Agreement, dated August 27, 2015 by and between LifeVantage Corporation, the Guarantors and lenders party thereto and TCW Special Situations, LLC as Collateral Agent and Administrative Agent

Filed herewith.
21.1

 List of Subsidiaries. Exhibit A to Form 10-KSB10-K for the fiscal year ended June 30, 20052014 filed on October 13, 2005.September 10, 2014.

23.1

 Consent of Ehrhardt Keefe Steiner & Hottman PC. Filed herewith.

24.1

 Power of Attorney Signature page to this reportreport.

31.1

 Certification of Chief Executive Officer pursuant to Section 302 of the Sarbanes-Oxley Act of 2002. Filed herewith.

31.2

 Certification of Chief Financial Officer pursuant to Section 302 of the Sarbanes-Oxley Act of 2002. Filed herewith.

32.1

 Certification of Chief Executive Officer pursuant to Section 906 of the Sarbanes-Oxley Act of 2002. Furnished herewith.

32.2

 Certification of Chief Financial Officer pursuant to Section 906 of the Sarbanes-Oxley Act of 2002. Furnished herewith.

 101*

101
 The following financial information from the registrant’s Annual Report on Form 10-K for the year ended June 30, 20122015 formatted in XBRL (eXtensible Business Reporting Language): (i) Condensed Consolidated Balance Sheets; (ii) Condensed Consolidated Statements of Operations and Other Comprehensive Income; (iii) Condensed Consolidated Statement of Stockholders’ Deficit; (iv) Condensed Consolidated Statements of Cash Flows; and (v) Notes to Condensed Consolidated Financial Statements, tagged as blocks of text. FurnishedFiled herewith.


- 49-



#Management contract or compensatory plan.
*Users
Confidential treatment has been granted by the SEC with respect to certain portions of these exhibits.

**
The Company has been granted confidential treatment for portions of this data are advised that pursuant to Rule 406Tagreement. Accordingly, certain portions of Regulation S-T, this XBRL information is being furnishedagreement have been omitted in the version filed with this report and notsuch confidential portions have been filed herewith for purposes of Section 18 ofwith the Securities Exchange Act of 1934, as amended, and Sections 11 or 12 of the Securities Act of 1933, as amended, and is not to be incorporated by reference into any filing, or part of any registration statement or prospectus, of LifeVantage Corporation, whether made before or after the date hereof, regardless of any general incorporation language in such filingSEC.

-46-



- 50-



LIFEVANTAGE CORPORATION

Index to Consolidated Financial Statements


F - 1



REPORT OF INDEPENDENT REGISTERED PUBLIC ACCOUNTING FIRM

The Board of Directors and Stockholders

LifeVantage Corporation

Sandy, Utah


We have audited the accompanying consolidated balance sheets of LifeVantage Corporation and subsidiaries (the Company)“Company”) as of June 30, 20122015 and 2011,2014, and the related consolidated statements of operations and comprehensive income, (loss),changes in stockholders’ equity (deficit), and cash flows for each of the years then ended. These financial statements are the responsibility of the Company’s management. Our responsibility is to express an opinion on these financial statements based on our audits.

We conducted our audits in accordance with the standards of the Public Company Accounting Oversight Board (United States). Those standards require that we plan and perform the audit to obtain reasonable assurance about whether the financial statements are free of material misstatement. An audit includes examining, on a test basis, evidence supporting the amounts and disclosures in the financial statements. An audit also includes assessing the accounting principles used and significant estimates made by management, as well as evaluating the overall financial statement presentation. We believe that our audits provide a reasonable basis for our opinion.

In our opinion, the financial statements referred to above present fairly, in all material respects, the consolidated financial position of LifeVantage Corporation and subsidiaries as ofthree-year period ended June 30, 2012 and 2011, and the consolidated results of their operations and their cash flows for each of the years then ended, in conformity with U.S. generally accepted accounting principles.

2015. We also have audited in accordance with the standards of the Public Company Accounting Oversight Board (United States), LifeVantage Corporation’sCompany’s internal control over financial reporting as of June 30, 2012,2015, based on criteria established inInternal Control-IntegratedControl - Integrated Framework (2013) issued by the Committee of Sponsoring Organizations of the Treadway Commission and our report dated September 10, 2012 expressed an unqualified opinion thereon.

/s/ Ehrhardt Keefe Steiner & Hottman PC

Denver, Colorado

September 10, 2012

REPORT OF INDEPENDENT REGISTERED PUBLIC ACCOUNTING FIRM

The Board of Directors and Stockholders

LifeVantage Corporation

We have audited LifeVantage Corporation’s (the Company) internal control over financial reporting as of June 30, 2012, based on criteria established inInternal Control-Integrated Framework issued by the Committee of Sponsoring Organizations of the Treadway Commission (the COSO criteria)(COSO). The Company’s management is responsible for these consolidated financial statements, for maintaining effective internal control over financial reporting, and for its assessment of the effectiveness of internal control over financial reporting included in the accompanying Management’s Report on Internal Control Overover Financial Reporting. Our responsibility is to express an opinion on these consolidated financial statements and an opinion on the Company’s internal control over financial reporting based on our audit.

audits.


We conducted our auditaudits in accordance with the standards of the Public Company Accounting Oversight Board (United States). Those standards require that we plan and perform the auditaudits to obtain reasonable assurance about whether the consolidated financial statements are free of material misstatement and whether effective internal control over financial reporting was maintained in all material respects. Our audits of the consolidated financial statements included examining, on a test basis, evidence supporting the amounts and disclosures in the consolidated financial statements, assessing the accounting principles used and significant estimates made by management, and evaluating the overall consolidated financial statement presentation. Our audit of internal control over financial reporting included obtaining an understanding of internal control over financial reporting, assessing the risk that a material weakness exists, and testing and evaluating the design and operating effectiveness of internal control based on the assessed risk. Our auditaudits also included performing such other procedures as we considered necessary in the circumstances. We believe that our audit providesaudits provide a reasonable basis for our opinion.

opinions.


A company’s internal control over financial reporting is a process designed to provide reasonable assurance regarding the reliability of financial reporting and the preparation of financial statements for external purposes in accordance with generally accepted accounting principles. A company’s internal control over financial reporting includes those policies and procedures that (1) pertain to the maintenance of records that, in reasonable detail, accurately and fairly reflect the transactions and dispositions of the assets of the company; (2) provide reasonable assurance that transactions are recorded as necessary to permit preparation of financial statements in accordance with generally accepted accounting principles, and that receipts and expenditures of the company are being made only in accordance with authorizations of management and directors of the company; and (3) provide reasonable assurance regarding prevention or timely detection of unauthorized acquisition, use, or disposition of the company’s assets that could have a material effect on the financial statements.


Because of its inherent limitations, internal control over financial reporting may not prevent or detect misstatements. Also, projections of any evaluation of effectiveness to future periods are subject to the risk that controls may become inadequate because of changes in conditions or that the degree of compliance with the policies or procedures may deteriorate.


In our opinion, the consolidated financial statements referred to above present fairly, in all material respects, the financial position of LifeVantage Corporation and subsidiaries as of June 30, 2015 and 2014, and the consolidated consolidated results of their operations and their cash flows for each of the years in the three-year period ended June 30, 2015, in conformity with accounting principles generally accepted in the United States of America. Also in our opinion, LifeVantage Corporation and subsidiaries maintained, in all material respects, effective internal control over financial reporting as of June 30, 2012,2015, based on criteria established in Internal Control - Integrated Framework (2013), issued by the COSO criteria.

We also have audited, in accordance with the standardsCommittee of Sponsoring Organizations of the Public Company Accounting Oversight Board (United States), the consolidated balance sheets of LifeVantage Corporation as of June 30, 2012 and 2011, and the related consolidated statements of operations and comprehensive income (loss), stockholders’ equity, and cash flows for each of the years then ended, and our report dated Treadway Commission (COSO).




EKS&H LLLP
September 13, 2012 expressed an unqualified opinion thereon.

/s/ Ehrhardt Keefe Steiner & Hottman PC

1, 2015

Denver, Colorado

September 10, 2012




F - 2



LIFEVANTAGE CORPORATION AND SUBSIDIARIES

CONSOLIDATED BALANCE SHEETS

   As of, 
   June 30, 2012  June 30, 2011 

ASSETS

   

Current assets

   

Cash and cash equivalents

  $24,647,585   $6,370,974  

Marketable securities, available for sale

   —      350,000  

Accounts receivable, net

   333,295    941,802  

Inventory

   11,352,789    2,124,663  

Current deferred income tax asset

   1,244,142   

Prepaid expenses and deposits

   1,250,156    487,812  
  

 

 

  

 

 

 

Total current assets

   38,827,967    10,275,251  

Long-term assets

   

Property and equipment, net

   1,996,849    227,811  

Intangible assets, net

   1,881,642    1,963,277  

Long-term deferred income tax asset

   1,479,273    —    

Deposits

   342,105    32,173  
  

 

 

  

 

 

 

TOTAL ASSETS

   44,527,836   $12,498,512  
  

 

 

  

 

 

 

LIABILITIES AND STOCKHOLDERS’ EQUITY (DEFICIT)

   

Current liabilities

   

Accounts payable

  $3,615,697   $799,210  

Commissions payable

   5,630,976    1,999,969  

Reserve for sales returns

   862,602    435,135  

Accrued bonuses

   2,287,208    782,852  

Income tax payable

   545,672    36,000  

Other accrued expenses

   2,932,070    1,423,370  

Customer deposits

   153,557    33,893  

Revolving line of credit and accrued interest

   —      433,984  

Short-term derivative liabilities

   —      7,435,883  
  

 

 

  

 

 

 

Total current liabilities

   16,027,782    13,380,296  

Long-term liabilities

   

Deferred rent

   216,885    21,017  

Derivative liabilities

   —      19,905,401  
  

 

 

  

 

 

 

Total liabilities

   16,244,667    33,306,714  
  

 

 

  

 

 

 

Commitments and contingencies

   

Stockholders’ equity (deficit)

   

Preferred stock — par value $0.001, 50,000,000 shares authorized, no shares issued or outstanding

   —      —    

Common stock — par value $0.001, 250,000,000 shares authorized and 110,174,030 and 98,794,499 issued and outstanding as of June 30, 2012 and 2011, respectively

   110,853    98,795  

Additional paid-in capital

   105,154,116    67,606,293  

Accumulated deficit

   (76,960,603  (88,453,607

Accumulated other comprehensive loss

   (21,197  (59,683
  

 

 

  

 

 

 

Total stockholders’ equity (deficit)

   28,283,169    (20,808,202
  

 

 

  

 

 

 

TOTAL LIABILITIES AND STOCKHOLDERS’ EQUITY (DEFICIT)

  $44,527,836   $12,498,512  
  

 

 

  

 

 

 

 June 30,
 2015 2014
(In thousands, except per share data)   
ASSETS   
Current assets   
Cash and cash equivalents$13,905
 $20,387
Accounts receivable1,031
 1,317
Income tax receivable2,179
 4,681
Inventory9,248
 8,826
Current deferred income tax asset1,117
 158
Prepaid expenses and deposits2,995
 4,604
Total current assets30,475
 39,973
    
Property and equipment, net5,759
 6,941
Intangible assets, net1,879
 2,014
Deferred debt offering costs, net1,098
 1,353
Long-term deferred income tax asset235
 1,285
Other long-term assets1,433
 2,433
TOTAL ASSETS$40,879
 $53,999
LIABILITIES AND STOCKHOLDERS’ EQUITY   
Current liabilities   
Accounts payable$2,614
 $2,854
Commissions payable6,505
 7,594
Other accrued expenses5,600
 7,554
Current portion of long-term debt11,141
 4,700
Total current liabilities25,860
 22,702
    
Long-term debt   
Principal amount10,484
 26,125
Less: unamortized discount(853) (1,052)
Long-term debt, net of unamortized discount9,631
 25,073
Other long-term liabilities2,063
 2,234
Total liabilities37,554
 50,009
Commitments and contingencies- Note 11
 
Stockholders’ equity   
Preferred stock — par value $0.001, 50,000 shares authorized, no shares issued or outstanding
 
Common stock — par value $0.001, 250,000 shares authorized and 97,671 and 102,173 issued and outstanding as of June 30, 2015 and 2014, respectively98
 102
Additional paid-in capital117,573
 115,244
Accumulated deficit(114,095) (111,240)
Accumulated other comprehensive loss(251) (116)
Total stockholders’ equity3,325
 3,990
TOTAL LIABILITIES AND STOCKHOLDERS’ EQUITY$40,879
 $53,999
The accompanying notes are an integral part of these consolidated financial statements.


F - 3



LIFEVANTAGE CORPORATION AND SUBSIDIARIES

CONSOLIDATED STATEMENTS OF OPERATIONS AND COMPREHENSIVE INCOME

   For the years ended, 
   June 30, 2012  June 30, 2011 

Sales, net

  $126,182,848   $38,919,223  

Cost of sales

   18,052,151    5,917,394  
  

 

 

  

 

 

 

Gross profit

   108,130,697    33,001,829  

Operating expenses:

   

Sales and marketing

   68,397,356    21,060,213  

General and administrative

   16,396,631    7,516,106  

Research and development

   1,359,055    508,603  

Depreciation and amortization

   521,271    214,703  
  

 

 

  

 

 

 

Total operating expenses

   86,674,313    29,299,625  
  

 

 

  

 

 

 

Operating income

   21,456,384    3,702,204  

Other expense:

   

Interest expense

   (44,234  (5,947,683

Change in fair value of derivative liabilities

   (6,740,525  (48,454,271
  

 

 

  

 

 

 

Total other expense

   (6,784,759  (54,401,954
  

 

 

  

 

 

 

Net income (loss) before income taxes

   14,671,625    (50,699,750
  

 

 

  

 

 

 

Income tax expense

   (2,202,548  (92,000
  

 

 

  

 

 

 

Net income (loss)

  $12,469,077   $(50,791,750
  

 

 

  

 

 

 

Net income (loss) per share, basic

  $0.12   $(0.69
  

 

 

  

 

 

 

Net income (loss) per share, diluted

  $0.11   $(0.69
  

 

 

  

 

 

 

Weighted average shares, basic

   102,695,919    73,173,498  

Weighted average shares, diluted

   118,330,898    73,173,498  

Other comprehensive income (loss), net of tax:

   

Foreign currency translation adjustment

   38,486    (27,906
  

 

 

  

 

 

 

Other comprehensive income (loss)

  $38,486   $(27,906
  

 

 

  

 

 

 

Comprehensive income (loss)

  $12,507,563   $(50,819,656
  

 

 

  

 

 

 

 For the years ended June 30,
 2015 2014 2013
(In thousands, except per share data)     
Revenue, net$190,336
 $213,968
 $208,178
Cost of sales28,010
 33,194
 31,845
Product recall costs
 
 4,798
Gross profit162,326
 180,774
 171,535
Operating expenses:     
Commissions and incentives91,074
 104,525
 101,737
Selling, general and administrative57,353
 56,801
 57,730
Total operating expenses148,427
 161,326
 159,467
Operating income13,899
 19,448
 12,068
Other income (expense):     
Interest expense(3,087) (3,177) (3)
Other income (expense), net(159) 384
 (912)
Total other income (expense)(3,246) (2,793) (915)
Income before income taxes10,653
 16,655
 11,153
Income tax expense(3,666) (5,272) (3,545)
Net income$6,987
 $11,383
 $7,608
Net income per share:     
Basic$0.07
 $0.11
 $0.07
Diluted$0.07
 $0.10
 $0.06
Weighted-average shares outstanding:     
Basic97,293
 105,791
 112,276
Diluted99,052
 111,599
 122,888
Other comprehensive loss, net of tax:     
Foreign currency translation adjustment(135) (3) (92)
Other comprehensive loss, net of tax:(135) (3) (92)
Comprehensive income$6,852
 $11,380
 $7,516
The accompanying notes are an integral part of these consolidated financial statements.


F - 4



LIFEVANTAGE CORPORATION AND SUBSIDIARIES

CONSOLIDATED STATEMENTS OF STOCKHOLDERS’ EQUITY (DEFICIT)

For the years ended June 30, 20122015, 2014, and 2011

  Common Stock  Additional
Paid In Capital
  Accumulated
Deficit
  Accumulated
Other
Comprehensive
Loss
  Total 
  Shares  Amount     

Balances, June 30, 2010

  61,494,849   $61,495   $21,457,145   $(37,661,857 $(31,777 $(16,174,994

Exercise of options and warrants

  9,448,251    9,448    13,091,039    —      —      13,100,487  

Conversion of debt to equity

  27,851,399    27,852    32,291,624    —      —      32,319,476  

Options/Warrants issued for services

  —      —      766,485    —      —      766,485  

Net loss

  —      —      —      (50,791,750  —      (50,791,750

Currency translation adjustment

  —      —      —      —      (27,906  (27,906
 

 

 

  

 

 

  

 

 

  

 

 

  

 

 

  

 

 

 

Balances, June 30, 2011

  98,794,499   $98,795   $67,606,293   $(88,453,607 $(59,683 $(20,808,202

Options/warrants issued for services

  —      —      1,322,565    —      —      1,322,565  

Exercise of options and warrants

  11,909,204    11,909    19,747,336    —      —      19,759,245  

Issuance of restricted stock

  149,253   149    (149  —      —      —    

Repurchase of company stock

  (678,926  —      —      (976,073  —      (976,073

Reclassification of liability warrants

  —      —      16,478,071    —      —      16,478,071  

Currency translation adjustment

  —      —      —      —      38,486    38,486  

Net income

  —      —      —      12,469,077    —      12,469,077  
 

 

 

  

 

 

  

 

 

  

 

 

  

 

 

  

 

 

 

Balances, June 30, 2012

  110,174,030   $110,853   $105,154,116   $(76,960,603 $(21,197 $28,283,169  
 

 

 

  

 

 

  

 

 

  

 

 

  

 

 

  

 

 

 

2013

 Common Stock 
Additional
Paid-In Capital
 
Accumulated
Deficit
 
Accumulated
Other
Comprehensive
Loss
 Total
 Shares Amount 
(In thousands)           
Balances, June 30, 2012110,174
 $111
 $105,154
 $(76,961) $(21) $28,283
Stock-based compensation
 
 2,169
 
 
 2,169
Exercise of options and warrants7,270
 7
 3,093
 
 
 3,100
Issuance of shares related to restricted stock2,616
 3
 (3) 
 
 
Repurchase of company stock(2,972) 
 
 (7,123) 
 (7,123)
Reclassification of liability warrants
 
 
 
 
 
Currency translation adjustment
 
 
 
 (92) (92)
Net income
 
 
 7,608
 
 7,608
Balances, June 30, 2013117,088
 $121
 $110,413
 $(76,476) $(113) $33,945
Stock-based compensation
 
 2,606
 
 
 2,606
Exercise of options and warrants5,185
 5
 2,225
 
 
 2,230
Issuance of shares related to restricted stock225
 
 
 
 
 
Shares canceled or surrendered as payment of tax withholding(686) 
 
 
 
 
Repurchase of company stock(19,639) (24) 
 (46,147) 
 (46,171)
Currency translation adjustment
 
 
 
 (3) (3)
Net income
 
 
 11,383
 
 11,383
Balances, June 30, 2014102,173
 $102
 $115,244
 $(111,240) $(116) $3,990
Stock-based compensation
 
 1,737
 
 
 1,737
Exercise of options and warrants2,630
 3
 593
 
 
 596
Issuance of shares related to restricted stock1,325
 1
 (1) 
 
 
Shares canceled or surrendered as payment of tax withholding(904) 
 
 
 
 
Repurchase of company stock(7,553) (8) 
 (9,842) 
 (9,850)
Currency translation adjustment
 
 
 
 (135) (135)
Net income
 
 
 6,987
 
 6,987
Balances, June 30, 201597,671
 $98
 $117,573
 $(114,095) $(251) $3,325
The accompanying notes are an integral part of these consolidated financial statements.


F - 5



LIFEVANTAGE CORPORATION AND SUBSIDIARIES

CONSOLIDATED STATEMENTS OF CASH FLOWS

   For the years ended June 30, 
   2012  2011 

Cash Flows from Operating Activities:

   

Net income (loss)

  $12,469,077   $(50,791,750

Adjustments to reconcile net income (loss) to net cash provided by operating activities:

   

Depreciation and amortization

   521,271    214,703  

Loss on disposal of equipment

   37,598    —    

Stock based compensation to employees

   1,188,735    670,073  

Stock based compensation to non-employees

   133,831    96,412  

Deferred income tax benefit

   (2,723,415  —    

Non-cash interest expense from convertible debentures

   —      4,746,905  

Non-cash interest expense from amortization of deferred offering costs

   —      844,792  

Change in fair value of derivative liabilities

   6,740,525    48,454,271  

Changes in operating assets and liabilities:

   

Decrease/(increase) in accounts receivable, net

   608,507    (540,205

(Increase) in inventory

   (9,228,126  (1,630,805

(Increase) in prepaid expenses and deposits

   (762,344  (333,948

(Increase) in deposits

   (309,932  (3,561

Increase in accounts payable

   2,816,487    28,269  

Increase/(decrease) in customer deposits

   119,664    (904

Increase in accrued expenses

   7,581,202    2,932,847  

Increase/(decrease) in deferred rent

   195,868    (6,174
  

 

 

  

 

 

 

Net Cash Provided by Operating Activities

   19,388,948    4,680,925  
  

 

 

  

 

 

 

Cash Flows from Investing Activities:

   

Redemption of marketable securities

   350,000    75,000  

Purchase of equipment

   (2,193,951  (122,303

Purchase of intangible assets

   (52,321  (41,664
  

 

 

  

 

 

 

Net Cash Used in Investing Activities

   (1,896,272  (88,967
  

 

 

  

 

 

 

Cash Flows from Financing Activities:

   

Net payments on revolving line of credit and accrued interest

   (433,984  —    

Excess tax benefits from stock based compensation

   387,614    —    

Issuance of common stock

   —      169,246  

Repurchase of company stock

   (976,073  —    

Exercise of options and warrants

   1,767,892    —    
  

 

 

  

 

 

 

Net Cash Provided by Financing Activities

   745,449    169,246  
  

 

 

  

 

 

 

Foreign Currency Effect on cash

   38,486    (27,906

Increase in cash and cash equivalents

   18,276,611    4,733,298  

Cash and Cash Equivalents — beginning of period

   6,370,974    1,637,676  
  

 

 

  

 

 

 

Cash and Cash Equivalents — end of period

   24,647,585    6,370,974  
  

 

 

  

 

 

 

 For the years ended June 30,
 2015 2014 2013
(In thousands)     
Cash Flows from Operating Activities:     
Net income$6,987
 $11,383
 $7,608
Adjustments to reconcile net income to net cash provided by operating activities:     
Depreciation and amortization2,285
 2,118
 1,659
Stock-based compensation1,806
 2,953
 2,169
Amortization of deferred financing fees255
 159
 
Amortization of debt discount198
 122
 
Impairment of inventory
 
 3,923
Deferred income tax91
 2,172
 (892)
Changes in operating assets and liabilities:     
Decrease/(increase) in receivables2,651
 (2,044) (3,653)
Decrease/(increase) in inventory(936) 1,646
 (3,356)
Decrease/(increase) in prepaid expenses and deposits1,486
 (2,318) (1,065)
Decrease/(increase) in long-term assets826
 (1,045) (1,168)
Increase/(decrease) in accounts payable(171) (2,384) 1,593
Increase/(decrease) in accrued expenses(2,170) (537) 3,403
Increase/(decrease) in other long-term liabilities(87) (120) 441
Net Cash Provided by Operating Activities13,221
 12,105
 10,662
Cash Flows from Investing Activities:     
Purchase of equipment(1,159) (1,898) (5,080)
Purchase of intangible assets
 (350) 
Net Cash Used in Investing Activities(1,159) (2,248) (5,080)
Cash Flows from Financing Activities:     
Proceeds from term loan
 45,825
 
Payment of deferred financing fees
 (1,511) 
Excess tax benefits from stock-based compensation128
 655
 1,406
Repurchase of company stock(9,850) (46,171) (7,123)
Payment on term loan(9,200) (16,175) 
Exercise of options and warrants468
 1,573
 1,694
Net Cash Used in Financing Activities(18,454) (15,804) (4,023)
Foreign Currency Effect on cash(90) 35
 92
Increase (Decrease) in cash and cash equivalents(6,482) (5,912) 1,651
Cash and Cash Equivalents — beginning of period20,387
 26,299
 24,648
Cash and Cash Equivalents — end of period13,905
 20,387
 26,299
The accompanying notes are an integral part of these consolidated financial statements.


F - 6



LIFEVANTAGE CORPORATION AND SUBSIDIARIES

CONSOLIDATED STATEMENTS OF CASH FLOWS

   For the years ended June 30, 
   2012   2011 

Non Cash Investing and Financing Activities:

    

Conversion of debt to common stock

   —      $5,570,280  

Conversion of derivative to common stock

   —      $26,749,195  

Exercise of warrant liabilities

  $17,603,738    $12,931,242  

SUPPLEMENTAL DISCLOSURE OF CASH FLOW INFORMATION

    

Cash paid for interest expense

   —      $384,893  

Cash paid for income taxes

  $3,701,000    $56,000  

For the year ended June 30, 2012 the Company issued 10,297,204 shares of common stock for a total exercise price of $5,994,929 through non-cash exercises of 12,562,859 warrants. For the year ended June 30, 2011 the Company issued 8,833,845 shares of common stock for a total exercise price of $6,394,700 through non-cash exercises of 12,929,979 warrants.

 For the years ended June 30,
 2015 2014 2013
Non Cash Investing and Financing Activities:     
Increase in property and equipment/other long-term liabilities$
 $1,386
 $359
SUPPLEMENTAL DISCLOSURE OF CASH FLOW INFORMATION     
Cash paid for interest$2,633
 $2,758
 $3
Cash paid for income taxes$1,658
 $4,879
 $6,090
Common stock shares issued upon cashless warrant exercises1,763

2,698

3,793
Total cashless exercise price of warrants$1,462

$1,615

$2,147
Gross warrants underlying cashless exercises2,924

3,409

4,564
The accompanying notes are an integral part of these consolidated financial statements.



F - 7



LIFEVANTAGE CORPORATION AND SUBSIDIARIES

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS



Note 1 — Organization and Basis of Presentation:

The Company

LifeVantage Corporation (“LifeVantage” oris a company dedicated to helping people achieve their health, wellness and financial independence goals. We provide quality, scientifically-validated products and a financially rewarding network marketing business opportunity to customers and independent distributors who seek a healthy lifestyle and financial freedom. We sell our products to independent distributors and preferred customers located in the “Company”) was formed underUnited States, Japan, Hong Kong, Australia, Canada, Philippines, Mexico, and Thailand.
We engage in the identification, research, development and distribution of advanced nutraceutical dietary supplements and skin care products, including Protandim®, our scientifically-validated dietary supplement, LifeVantage TrueScience®, our line of anti-aging skin care products, Canine Health®, our companion pet supplement formulated to combat oxidative stress in dogs, and Axio®, our energy drink mixes.
We were incorporated in Colorado law in June 1988 under the name Andraplex Corporation. The Company amended itsWe changed our corporate name to Yaak River Resources, Inc. in January 1992, and subsequently changed it again in October 2004 to Lifeline Therapeutics, Inc. in October 2004 and to LifeVantage Corporation in November 2006. The Company is in the business of marketing and selling its proprietary products, primarily Protandim®, to individuals throughout the United States and in Japan, Canada and Mexico. LifeVantage is a Colorado corporation with its corporate office in Sandy, Utah.

On October 26, 2004, the Company consummated an Agreement and Plan of Reorganization with Lifeline Nutraceuticals Corporation (“LNC”), a privately held Colorado corporation, formed on July 1, 2003. In October 2004 and March 2005, we acquired all of the shareholders of LNC exchanged 81% of their outstanding shares of common stock for 15,385,110 shares of common stock of the Company, which represented 94% of the then issued and outstanding shares of the Company. The Company assumed the obligations of LNC note holders as part of the transaction.

Lifeline Nutraceuticals Corporation. In July 2009 the Company formed the wholly owned subsidiariesNovember 2006, we changed our name to LifeVantage de México, S. de R.L. de C.V. (Limited Liability Company), Importadora LifeVantage, S. de R.L. de C.V. (Limited Liability Company), and Servicios Administrativos para la Importación de Productos Body & Skin, S.C. to conduct business in Mexico.

In January 2012, the Company formed LifeVantage Asia Pte. Ltd. (“LifeVantage Asia”) and LifeVantage Australia Pty. Ltd. (“LifeVantage Australia”). LifeVantage Asia is a wholly-owned subsidiary of the Company and LifeVantage Australia is a wholly-owned subsidiary of LifeVantage Asia. In February 2012, the Company formed LifeVantage Hong Kong Pte. Ltd. (“LifeVantage Hong Kong”) and LifeVantage Japan K.K. (“LifeVantage Japan”). LifeVantage Hong Kong and LifeVantage Japan are both wholly-owned subsidiaries of LifeVantage Asia.

Corporation.

Note 2 — Summary of Significant Accounting Policies

Consolidation

The consolidated financial statements include the accounts of the Company and its wholly-owned subsidiaries. All significant intercompany accounts and transactions are eliminated in consolidation.

Reclassifications

The prior year amount for accrued bonuses During fiscal 2014, the Company combined the line items sales and marketing, general and administrative, research and development, and depreciation and amortization into two line items on the balance sheet hasconsolidated statements of operations and comprehensive income, namely, commissions and incentives and selling, general and administrative to have a presentation that is more comparable to that of the Company’s peers. The Company reclassified prior period line items to conform to the current period presentation. Certain other prior period balances have also been reclassified to conform to the current yearperiod presentation.

Use of Estimates

We prepare our consolidated financial statements and related disclosures in conformity with accounting principles generally accepted in the United States of America (GAAP). In preparing these statements, we are required to use estimates and assumptions that affect the reported amounts of assets and liabilities, the disclosure of contingent assets and liabilities at the date of the financial statements and the reported amounts of revenues and expenses during the reporting period. Actual results could differ materially from those estimates and assumptions. On an ongoing basis, we review our estimates, including those related to allowances for inventory obsolescence, sales returns, income taxes and tax valuation reserves, share-based compensation, derivative liabilities and loss contingencies.

Foreign Currency Translation
A portion of the Company’s business operations occurs outside the United States. The local currency of each of the Company’s subsidiaries is generally its functional currency. All assets and liabilities are translated into U.S. dollars at exchange rates existing at the balance sheet dates, revenue and expenses are translated at weighted-average exchange rates and stockholders’ equity is recorded at historical exchange rates. The resulting foreign currency translation adjustments are recorded as a separate component of stockholders’ equity in the consolidated balance sheets. Transaction gains and losses are included in other income (expense), net in the consolidated statements of operations and comprehensive income.
Fair Value of Financial Instruments

Accounting guidance on fair value measurements and disclosures requires disclosures about the fair value for all financial instruments, whether or not recognized, for financial statement purposes. Disclosures about fair

value of financial instruments are based on pertinent information available to management as of June 30, 20122015 and 2011.2014. Accordingly, the estimates presented in these consolidated financial statements are not necessarily indicative of the amounts that could be realized on disposition of the financial instruments.


F - 8



Management has estimated the fair values of cash marketable securities,and cash equivalents, accounts receivable, accounts payable, commissions payable and other accrued expenses to be approximatelyapproximate their respective carrying values reported in these consolidated financial statements because of their short maturities.

Fair Value Measurements

Fair value measurement requirements are embodied in certain accounting standards applied in the preparation of our financial statements. Significant fair value measurements resulted from the application of guidance on fair value measurements and disclosures of our common stock and warrant financing arrangements and to our share-based payment arrangements. Accounting guidance on fair value measurements and disclosures establishes a framework and hierarchy for measuring fair value.

Fair value hierarchy:

(1)Level 1 inputs are quoted prices in active markets for identical assets and liabilities.

(2)Level 2 inputs are inputs which include quoted prices for similar assets and liabilities in active markets and inputs that are observable for the assets or liabilities, either directly or indirectly, for substantially the full term of the financial instrument.

(3)Level 3 inputs are unobservable inputs and are significant to the fair value measurement.

Accounting guidance on fair value measurement and disclosures permits entities to choose to measure financial instruments and certain other items at fair value. It was effective for our year beginning July 1, 2008. Upon its adoption and at this time, we do not intend to reflect any of our current financial instruments at fair value (except that we are required to carry our derivative financial instruments at fair value). However, we will consider the appropriateness of recognizing financial instruments at fair value on a case by case basis in future periods.

There were no financial instruments measured at fair value as of June 30, 2012. The summary of fair values of financial instruments as of June 30, 2011 is as follows:

June 30, 2011

 

Instrument

  Fair Value   Carrying Value   Level   Valuation Methodology 

Marketable Securities

  $350,000    $350,000     2     Market Price  

Derivative warrant liabilities

  $27,341,284    $27,341,284     3     
 
Dilution Adjusted
Black-Scholes
  
  

Embedded conversion liability

  $—      $—       3     Lattice model  

The following represents a reconciliation of the changes in fair value of financial instruments measured at fair value on a recurring basis using significant unobservable inputs (Level 3) for the years ended June 30, 2012 and 2011:

   June 30, 2012  June 30, 2011 

Beginning balance: Derivative liabilities

  $27,341,284   $18,567,450  

Total losses

   6,740,525    48,454,271  

Reclassification of liability to equity

   (16,478,071  —    

Purchases, sales, issuances and settlements, net

   (17,603,738  (39,680,437
  

 

 

  

 

 

 

Ending balance: Derivative liabilities

  $—     $27,341,284  
  

 

 

  

 

 

 

Cash and Cash Equivalents

The Company considers only its monetary liquid assets with original maturities of three months or less to be cash and cash equivalents.

Accounts Receivable

The Company’s accounts receivable for the years ended June 30, 20122015 and 20112014 consist primarily of credit card receivables. Based on the Company’s verification process for customer credit cards and historical information available, management has determined that an allowance for doubtful accounts on credit card sales related to its direct and independent distributorcustomer sales as of June 30, 20122015 or 2014 is not necessary. No bad debt expense has been recorded for the years ended June 30, 20122015, 2014, and 2011.

2013.

Inventory
As of

Inventory is statedJune 30, 2015 and 2014, inventory consisted of (in thousands):

 June 30,
 2015 2014
Finished goods$5,783
 $4,749
Raw materials3,465
 4,077
Total inventory$9,248
 $8,826
Inventories are carried and depicted above at the lower of cost or market, value. Cost is determined using the first-in, first-out method. The Company has capitalized payments to its contract manufacturer for the acquisitionmethod, which includes a reduction in inventory values of raw materials$0.3 million and commencement of the manufacturing, bottling and labeling of the Company’s product. The Company had no work-in-process inventory$0.7 million at June 30, 2012 or 2011. As of June 30, 20122015 and June 30, 2011, inventory consisted of:

   June 30, 
   2012   2011 

Finished goods

  $5,964,134    $736,103  

Raw materials

   5,388,655     1,388,560  
  

 

 

   

 

 

 

Total inventory

  $11,352,789    $2,124,663  
  

 

 

   

 

 

 

2014, respectively, related to obsolete and slow-moving inventory.

Property and Equipment

Property and equipment are recorded at cost. Depreciation of propertycost and equipment is expensed in amounts sufficient to relate the expiring costs of depreciable assets to operations over estimated useful lives,depreciated using the straight-line method. method over the following useful lives:
Years
Equipment (includes computer hardware and software)3
Furniture and fixtures5
Leasehold improvements*
Vehicles5
*Leasehold improvements are depreciated over the shorter of estimated useful liveslife of the related asset or the lease term. Estimated useful lives range from three to five years. When such assets are sold or otherwise disposed of, the cost and accumulated depreciation are removed from the accounts, and any resulting gain or loss is reflected in operations in the period of disposal.
The cost of normal maintenance and repairs is charged to expense as incurred. When an asset is sold or otherwise disposed of, the cost and associated accumulated depreciation are removed from the accounts and the resulting gain or loss is recognized in the consolidated statements of operations and comprehensive income. Significant expenditures that increase the useful life of an asset are capitalized and depreciated over the estimated useful life of the asset. Property and equipment consist of:

   June 30, 
   2012  2011 

Equipment

  $1,972,306   $471,962  

Software

   687,242    96,503  

Accumulated depreciation

   (662,699  (340,654
  

 

 

  

 

 

 

Property and equipment, net

  $1,996,849   $227,811  
  

 

 

  

 

 

 

Depreciation expense totaled $387,315 and $90,845are reviewed for impairment whenever events or changes in circumstances indicate that the years ended June 30, 2012 and 2011, respectively.

carrying amount of such assets may not be recoverable. An impairment loss is recognized if the carrying amount of the asset exceeds its fair value.

Intangible Assets

The costs of applying for patents

Intangible assets are capitalized and, once the patent is granted, will bestated at cost less accumulated amortization. Definite-lived intangible assets are amortized onover their related useful lives, using a straight-line basis overmethod, consistent with the lesserunderlying expected future cash flows related to the specific intangible asset. Definite-lived intangible assets are reviewed for impairment whenever events or changes in circumstances exist that indicate the carrying amount of an asset may not be recoverable. When indicators of impairment exist, an estimate of undiscounted net cash flows is used in measuring whether the carrying amount of the patent’s economicasset or legal life. Capitalized costs will be expensedrelated asset group is recoverable. Measurement of the amount of impairment, if

patents any, is based upon the difference between the asset’s carrying value and estimated fair value.


F - 9



Indefinite-lived intangible assets are not grantedamortized; however, they are tested at least annually for impairment or itmore frequently if events or changes in circumstances exist that may indicate impairment. An impairment loss is determined that the patent is impaired. The Company reviewsrecognized if the carrying value of its patent costs periodically to determine whether the patents have continuing value and such reviews could result in impairmentamount of the recorded amounts. As of June 30, 2012, four U.S. patents have been granted, which are being amortized beginning upon the date of the grant and continuing over their remaining legal lives. Trademarks are not amortized, rather they are subject to annual impairment tests.asset exceeds its fair value. Annual impairment tests were completed resulting in no impairment charges for any of the periods shown. As of June 30, 2012 and June 30, 2011, intangible assets consisted of:

   June 30, 
   2012  2011 

Patent costs

  $2,321,186   $2,290,558  

Trademark costs

   201,813    180,120  

Accumulated amortization

   (641,357  (507,401
  

 

 

  

 

 

 

Intangible assets, net

  $1,881,642   $1,963,277  
  

 

 

  

 

 

 

Amortization expense totaled $133,956 and $123,858 for the years ended June 30, 2012 and 2011, respectively.

Impairment of Long-Lived Assets

Pursuant to guidance established for impairment or disposal of assets, the Company assesses impairment whenever events or changes in circumstances indicate that the carrying amount of a long-lived asset may not be recoverable. When an assessment for impairment of long-lived assets, long-lived assets to be disposed of, and certain identifiable intangibles related to those assets is performed, the Company is required to compare the net carrying value of long-lived assets on the lowest level at which cash flows can be determined on a consistent basis to the related estimates of future undiscounted net cash flows for such assets. If the net carrying value exceeds the net cash flows, then an impairment is recognized to reduce the carrying value to the estimated fair value, generally equal to the future discounted net cash flow. For the years ended June 30, 20122015 and 20112014 management has concluded that there are no indications of impairment.

Concentration of Credit Risk

Accounting guidance for financial instruments requires disclosure of significant concentrations of credit risk regardless of the degree of such risk. Financial instruments with significant credit risk include cash and marketable securities.cash equivalents. At June 30, 2012,2015, the Company had $18,354,156$10.6 million in cash accounts at one financial institution $1,292,685and $3.3 million in foreign banks for our Mexico and Japan related businesses and $5,000,745 in an investment management account at anotherother financial institution.institutions. As of June 30, 20122015 and 20112014 and periodically throughoutduring the yearyears then ended, the Company’s cash balances exceeded federally insured limits.

Revenue Recognition

We ship

The Company ships the majority of ourits product directly to the consumer via UPS and receivereceives substantially all payment for these sales in the form of credit card receipts. Revenue from direct product sales to customers is recognized upon passage of title and risk of loss to customers when product is shipped from the fulfillment facility.loss. Estimated returns are recorded when product is shipped. TheSubject to some exceptions based on local regulations, the Company’s return policy is to provide a 30-day money back guarantee on orders placed by customers.full refund for product returned within 30 days if the returned product is unopened or defective. After 30 days, the Company generally does not issue refunds to direct sales customers for returned product. In the network marketing sales channel, theThe Company allows terminating distributors to return up to 30% of unopened, unexpired product that they have purchased within the prior twelve months subject to certain consumption limitations.for a full refund, less a 10% restocking fee. The Company establishes the returns reserve based on historical experience. The returns reserve is evaluated on a quarterly basis. As of June 30, 20122015 and June 30, 2011,2014, the Company’s reserve balance for returns and allowances was $862,602$0.1 million and $435,135,$0.6 million, respectively.

Commissions and Incentives
Commissions and incentives expenses are the Company’s most significant expenses and are classified as operating expenses. Commissions and incentives expenses include sales commissions paid to our independent distributors, special incentives, costs for incentive trips and other rewards. Commission and incentive expenses do not include any amounts we pay to our independent distributors for personal purchases. Commissions paid to independent distributors on personal purchases are considered a sales discount and are reported as a reduction to our net revenue.
Shipping and Handling

Shipping and handling costs associated with inbound freight and freight out to customers, including independent distributors, are included in cost of sales. Shipping and handling fees charged to all customers are included in sales.

Research and Development Costs

The Company expenses all costs related to research and development activities as incurred. Research and development expenses for the years ended June 30, 20122015, 2014, and 20112013 were $1,359,055$2.4 million, $2.0 million, and $508,603,$2.9 million respectively.

Stock-Based Compensation

The Company began usingrecognizes stock-based compensation by measuring the cost of services to be rendered based on the grant date fair value of the equity award. The Company recognizes stock-based compensation, net of any estimated forfeitures, over the period an employee is required to provide service in exchange for the award, generally referred to as the requisite service period. For awards with market based performance conditions, the cost of the awards is recognized as the requisite service is rendered by employees, regardless of when, if ever, the market based performance conditions are satisfied.
The Black-Scholes option pricing model is used to estimate the fair value approach, effective beginning in the first quarter of fiscal 2007, to account for stock-based compensation, in accordance with the modified versionstock options. The determination of prospective application as prescribed by accounting guidance on stock compensation.

The Company adopted and the shareholders approved the Company’s 2007 Long-Term Incentive Plan (the “2007 Plan”), effective November 21, 2006, to provide incentives to certain employees, officers, directors and consultants who contribute to the strategic and long-term performance objectives and growth of the Company. A maximum of 10,000,000 shares of the Company’s common stock can be issued under the 2007 Plan in connection with the grant of awards. Awards to purchase common stock have been granted pursuant to the 2007 Plan and are outstanding to various employees, officers, directors, Scientific Advisory Board (“SAB”) members and independent distributors at prices between $0.21 and $1.50 per share, with initial vesting periods that ranged from one to three years. Awards expire in accordance with the terms of each award and the shares subject to the award are added back to the 2007 Plan upon expiration of the award. As of June 30, 2012 there were awards outstanding, net of awards expired, for the purchase in aggregate of 6,927,160 shares of the Company’s common stock. As of June 30, 2012 there were 26,269 shares available for issuance under the 2007 Plan.

The Company adopted and the shareholders approved the Company’s 2010 Long-Term Incentive Plan (the “2010 Plan”), effective November 19, 2010, to provide incentives to certain employees, officers, directors and consultants who contribute to the strategic and long-term performance objectives and growth of the Company. A maximum of 6,900,000 shares of the Company’s common stock can be issued under the 2010 Plan in connection with the grant of awards. Awards to purchase common stock have been granted pursuant to the 2010 Plan and are outstanding to various employees, officers and directors at prices between $0.63 and $3.53, vesting over one to four year periods. As of June 30, 2012 there were awards outstanding, net of awards expired, for the purchase in aggregate of 4,029,836 shares of the Company’s common stock. As of June 30, 2012 there were 2,510,164 shares available for issuance under the 2010 Plan.

Compensation expense was calculated using the fair value method duringof stock options is affected by the fiscal years ended June 30, 2012Company's stock price and 2011 usinga number of assumptions, including expected volatility, expected life, risk-free interest rate and expected dividends. The Company uses historical volatility as the expected volatility


F - 10



assumption required in the Black-Scholes option pricing model. The following assumptions were used for options and warrants granted during the years ended June 30, 2012 and 2011:

1.risk-free interest rate of between 0.59 and 1.41 percent in fiscal 2012 and between 1.33 and 2.64 percent in fiscal 2011;

2.dividend yield of -0- percent in fiscal 2012 and 2011;

3.expected life of 3.0 to 6.65 years in fiscal 2012 and 2011;

4.a volatility factor of the expected market price of the Company’s common stock of between 119 and 137 percent in fiscal 2012 and between 125 and 129 percent in fiscal 2011.

The Company follows Staff Accounting Bulletin (“SAB”) 107 guidance to estimate the expected life of the options. The guidance providesutilizes a simplified method for estimating the expected life of the options. The Company uses this method because it believes that it provides a better estimate than the Company’s historical data as post vesting exercises have been limited.

The risk-free interest rate assumption is based on observed interest rates appropriate for the expected terms of the stock options.

The fair value of restricted stock grants is based on the closing market price of the Company's stock on the date of grant less the Company's expected dividend yield. The fair value of performance stock units that include market based performance conditions is based on the closing market price of the Company's stock on the date of grant less the Company's expected dividend yield, with further adjustments made to reflect the market conditions that must be satisfied in order for the units to vest by using a Monte-Carlo simulation model. Key assumptions for the Monte-Carlo simulation model include the risk-free rate, expected volatility, expected dividends and the correlation coefficient. The fair value of cash-settled performance-based awards, accounted for as liabilities, is remeasured at the end of each reporting period and is based on the closing market price of the Company’s stock on the last day of the reporting period. The Company recognizes compensation costs for these awards with performance conditions when it concludes it is probable that the performance conditions will be achieved. The Company reassesses the probability of vesting at each balance sheet date and adjusts compensation costs accordingly.
Income Taxes

Income taxes are accounted for under the asset and liability method. Deferred tax assets and liabilities are recognized for the future tax consequences attributable to differences between the financial statement carrying amounts of existing assets and liabilities and their respective tax bases and operating loss and tax credit carry-forwards. Deferred tax assets and liabilities are measured using statutory tax rates expected to apply to taxable income in the years in which those temporary differences are expected to be recovered or settled. The effect on deferred tax assets and liabilities from a change in tax rates is recognized in income in the period that includes the effective date of the change. In December 2011, we determined it was more likely than not that the deferred tax asset would be realized and as a result we released the valuation allowance we had established resulting in a net benefit of $2,802,000 which represents the benefit expected to be realized in future years.

The Company recognizes tax benefits from an uncertain position only if it is more likely than not that the position will be sustained upon examination by taxing authorities based on the technical merits of the issue. The amount recognized is the largest benefit that the Company believes has greater than a 50% likelihood of being realized upon settlement.

Income (Loss) Per Share

Basic income (loss) per share is computed by dividing the net income or loss by the weighted averageweighted-average number of common shares outstanding during the period.period, less unvested restricted stock awards. Diluted income (loss) per common share is computed by dividing net income (loss) by the weighted averageweighted-average common shares and potentially dilutive common share equivalents. equivalents using the treasury stock method.
The effects of approximately 363.1 million and 0.3 million common shares issuable upon exercise of options and non-vested shares of restricted stock outstanding as of June 30, 2011 pursuant to the convertible debentures2015 and warrants issued in the Company’s private placement offerings, compensation based warrants issued by the Company and the Company’s 2007 and 2010 Long-Term Incentive Plans2014, respectively, are not included in the computations whenas their effect is antidilutive. Because the Company incurred a net loss for the year ended June 30, 2011 the basic and diluted average outstanding shares are the same, as including the additional potential common share equivalents would have an antidilutive effect on the loss per share calculation.

was anti-dilutive.

The following is a reconciliation of earnings per share and the weighted-average common shares outstanding for purposes of computing basic and diluted net income per share:

   Year ended June 30, 
   2012   2011 

Numerator:

    

Net income (loss)

  $12,469,077    $(50,791,750

Denominator:

    

Basic weighted-average common shares outstanding

   102,695,919     73,173,498  

Effect of dilutive securities:

    

Stock awards and options

   5,516,411     —    

Warrants

   10,118,568     —    
  

 

 

   

 

 

 

Diluted weighted-average common shares outstanding

   118,330,898     73,173,498  
  

 

 

   

 

 

 

Basic

  $0.12    $(0.69
  

 

 

   

 

 

 

Diluted

  $0.11    $(0.69
  

 

 

   

 

 

 

Foreign currency translation

A portion of the Company’s business operations occurs outside the United States. The local currency of each of the Company’s subsidiaries is considered its functional currency. All assets and liabilities are translated into U.S. dollars at exchange rates existing at the balance sheet dates, revenue and expenses are translated at weighted-average exchange rates and stockholders’ equity is recorded at historical exchange rates. The resulting foreign currency translation adjustments are recorded as a separate component of stockholders’ equity in the consolidated balance sheets and transaction gains and losses are included in other income and expense in the consolidated financial statements.

share (in thousands, except per share amounts):

 Years ended June 30,
 2015 2014 2013
Numerator:     
Net income$6,987
 $11,383
 $7,608
Denominator:     
Basic weighted-average common shares outstanding97,293
 105,791
 112,276
Effect of dilutive securities:     
Stock awards and options1,264
 2,652
 3,832
Warrants495
 3,156
 6,780
Diluted weighted-average common shares outstanding99,052
 111,599
 122,888
Basic$0.07
 $0.11
 $0.07
Diluted$0.07
 $0.10
 $0.06

F - 11



Segment Information

The Company operates in a single operating segment by selling products to a globalan international network of independent distributors that operates in a seamlessan integrated manner from market to market. SellingCommissions and incentives expenses are the Company’s largest expense comprised of the commissions paid to its worldwide independent distributors. The Company manages its business primarily by managing its globalinternational network of independent distributors. The Company does not use profitability reports on a regional or divisional basis for making business decisions. However, the Company does report revenue in two geographic regions: Americas and Asia/Pacific. Substantially all long-lived assets are located in the U.S. Revenues by geographic area are as follows:

   Years ended June 30, 
   2012   2011 

Americas

  $90,121,702    $31,625,250  

Asia/Pacific

   36,061,146     7,293,973  
  

 

 

   

 

 

 

Total revenues

  $126,182,848    $38,919,223  
  

 

 

   

 

 

 

follows (in thousands):

 Years ended June 30,
 2015 2014 2013
Americas$138,118
 $141,227
 $133,046
Asia/Pacific52,218
 72,741
 75,132
Total revenues$190,336
 $213,968
 $208,178
Additional information as to the Company’s revenue from operations in the most significant geographical areas is set forth below:

   Years ended June 30, 
   2012   2011 

United States

  $89,230,031    $31,218,035  

Japan

   35,449,236     7,293,973  

below (in thousands):

 Years ended June 30,
 2015 2014 2013
United States$132,831
 $136,758
 $131,508
Japan$41,428
 $61,872
 $69,492
As of June 30, 2015 long-lived assets were $6.5 million in the U.S. and $1.5 million in Japan. As of June 30, 2014 long-lived assets were $9.8 million in the U.S. and $2.3 million in Japan.
Major Products
The Company's revenues are largely attributed to two product lines, Protandim® and the LifeVantage TrueScience® skin care regimen, which each accounted for more than 10% of total revenues for each of the years ended June 30, 2015, 2014 and 2013. On a combined basis, these products represent approximately 83.7%, 88.5% and 87.1% of our worldwide gross revenues for the years ended June 30, 2015, 2014 and 2013, respectively. The following table shows revenues by major product line for the years ended June 30, 2015, 2014 and 2013.
 For the years ended June 30,
 2015 2014 2013
Protandim®$120,967
 63.6% $142,935
 66.8% $138,996
 66.8%
LifeVantage TrueScience® skin care regimen38,287
 20.1% 46,474
 21.7% 42,229
 20.3%
Other31,082
 16.3% 24,559
 11.5% 26,953
 12.9%
Total$190,336
 100.0% $213,968
 100.0% $208,178
 100.0%
New Accounting Pronouncements

In May 2011,August 2014, FASB issued Accounting Standards Update (ASU) No. 2014-15 Preparation of Financial Statements - Going Concern (Subtopic 205-40), Disclosure of Uncertainties about an Entity’s Ability to Continue as a Going Concern. Under GAAP, continuation of a reporting entity as a going concern is presumed as the basis for preparing financial statements unless and until the entity’s liquidation becomes imminent. Preparation of financial statements under this presumption is commonly referred to as the going concern basis of accounting. If and when an entity’s liquidation becomes imminent, financial statements should be prepared under the liquidation basis of accounting in accordance with Subtopic 205-30, Presentation of Financial Statements-Liquidation Basis of Accounting. Even when an entity’s liquidation is not imminent, there may be conditions or events that raise substantial doubt about the entity’s ability to continue as a going concern. In those situations, financial statements should continue to be prepared under the going concern basis of accounting, but the amendments in this Update should be followed to determine whether to disclose information about the relevant conditions and events. The amendments in this Update are effective for the annual period ending after December 15, 2016, and for annual periods and interim periods thereafter. Early application is permitted. The Company will evaluate the going concern considerations in this ASU, but has not elected early application. However, as of and for the current period, management does

F - 12



not believe that conditions exist or events have occurred that would require additional disclosure under the amendments in this update.
In January 2015, FASB issued ASU 2011-04, Fair Value Measurement (Topic 820)No. 2015-01, Income Statement - Extraordinary and Unusual Items (Subtopic 225-20): Amendments to Achieve Common Fair Value Measurement and Disclosure Requirements in U.S. GAAP and IFRS. ASU 2011-04 provides a consistent definitionSimplifying Income Statement Presentation by Eliminating the Concept of fair value and ensures that the fair value measurement and disclosure requirements are similar between U.S. GAAP and International Financial Reporting Standards. ASU 2011-04 changes certain fair value measurement principles and enhances the disclosure requirements particularly for Level 3 fair value measurements.Extraordinary Items. This guidance eliminates from GAAP the concept of extraordinary and unusual items, and is effective for annual periods and interim andperiods within those annual reporting periods beginning after December 15, 2011, and will be applied prospectively.2015. Early application is permitted. The Company is currently evaluatingdoes not anticipate that the impactadoption of adopting ASU 2011-04, but believes therethis guidance will be no significanthave a material impact on its consolidated financial statements.

In June 2011, theApril 2015, FASB issued ASU 2011-05 as amended by ASU 2011-12, No. 2015-03, Interest - Imputation of Interest (Subtopic 825-30): Simplifying the Presentation of Comprehensive Income. ASU 2011-05Debt Issuance Costs. This guidance requires entitiesthat debt issuance costs related to present itemsa recognized debt liability be presented in the balance sheet as a direct deduction from the carrying amount of net incomethat debt liability, consistent with debt discounts. This update will become effective for the Company in the first quarter of fiscal 2016 and other comprehensive income either in one continuous statement, referred to as the statement of comprehensive income, or in two separate, but consecutive, statements of net income and other comprehensive income.requires retrospective application. The Company has early adopted this guidance effective September 30, 2011.

In July 2012, the Financial Accounting Standards Board (“FASB”) issued Accounting Standards Update (“ASU”) No. 2012-02 “Intangibles – Goodwill and Other (Topic 350): Testing Indefinite-Lived Intangible Assetsfor Impairment,” which permits an entity to first assess qualitative factors to determine whether it is more likely than not that an indefinite-lived intangible asset is impaired before performing quantitative impairment testing.

The amendments do not change the measurement of impairment losses. This update is effective for fiscal years beginning after September 15, 2012, with early adoption permitted. Management does not expectanticipate that the adoption of this ASU toguidance will have a material impact on its consolidated financial statements.

In July 2015, FASB issued ASU No. 2015-11, Inventory (Topic 330): Simplifying the Company’s resultsMeasurement of operations,Inventory. This guidance requires an entity to measure in scope inventory at the lower of cost and net realizable value. Net realizable value is the estimated selling prices in the ordinary course of business, less reasonably predictable costs of completion, disposal, and transportation. The amendments in this update are effective for annual periods and interim periods within those annual periods beginning after December 15, 2016. The Company does not anticipate that the adoption of this guidance will have a material impact on its consolidated financial position or cash flow.

statements.

Note 3 — LineProperty and Equipment
Property and equipment consist of Credit(in thousands):
 June 30,
 2015 2014
Equipment (includes computer hardware and software)$6,895
 $6,354
Furniture and fixtures1,481
 1,428
Leasehold improvements3,324
 3,095
Vehicles51
 142
Accumulated depreciation(5,992) (4,078)
Total property and equipment, net$5,759
 $6,941
Depreciation expense totaled

We established a line of credit to borrow up to 80% of our investments in certain marketable securities. The line was collateralized by$2.3 million, $2.0 million, and $1.5 million for the proceeds of the repurchase of the marketable securities. The line was paid in full in January 2012, in conjunction with the settlement of the marketable securitiesyears ended June 30, 2015, 2014, and is now closed.

2013, respectively.

Note 4 — Stockholders’ EquityIntangible Assets
Intangible assets consist of (in thousands):
 June 30,
 2015 2014
Patent costs$2,330
 $2,330
Accumulated amortization(1,046) (911)
Total definite-lived intangible assets, net1,284
 1,419
    
Trademarks and other indefinite-lived intangible assets595
 595
Total intangible assets, net$1,879
 $2,014
Amortization expense totaled

$0.1 million, $0.1 million, and $0.1 million for the years ended June 30, 2015, 2014, and 2013 respectively. Annual estimated amortization expense is expected to approximate $0.1 million for each of the five succeeding fiscal years.


F - 13



Note 5 — Other Accrued Expenses
Other accrued expenses consist of (in thousands):
 June 30,
 2015 2014
Accrued severance$638
 $150
Accrued incentives and promotions to distributors380
 829
Accrued payroll and other employee expenses583
 1,382
Deferred revenue990
 887
Accrued payable to vendors1,019
 910
Other taxes payable809
 1,894
Accrued other expenses1,181
 1,502
Total other accrued expenses$5,600
 $7,554
Note 6 — Long-Term Debt
On October 18, 2013 the Company entered into a Financing Agreement providing for a term loan facility in an aggregate principal amount of $47 million (the “Term Loan”) and a delayed draw term loan facility in an aggregate principal amount not to exceed $20 million (the “Delayed Draw Term Loan” and collectively with the Term Loan, the “Credit Facility”). The Delayed Draw Term Loan was available for borrowing in specified minimum amounts from time to time beginning after the effective date (as defined in the Financing Agreement) until October 18, 2014 or until the Delayed Draw Term Loan is reduced to zero, if earlier. The Company did not borrow any amounts under the Delayed Draw Term Loan.
On May 1, 2015 the Company entered into an Amendment No 1 to Financing Agreement ("Amendment No. 1"). Amendment No. 1 revised the March 31, 2015 and June 30, 2015 consolidated EBITDA covenants from $20.6 million and $21.3 million, respectively, to $17.0 million for each quarter end. Amendment No. 1 also revised the minimum unrestricted cash and cash equivalents that the Company is required to hold from $10.0 million to $8.0 million for the reporting periods ended March 31, 2015 and June 30, 2015. In addition, Amendment No. 1 required that the Company make accelerated principal payments on the Term Loan totaling $4.5 million during the fourth quarter of fiscal year 2015.
On August 27, 2015 the Company entered into an Amendment No. 2 to Financing Agreement ("Amendment No. 2" and collectively, with the Term Loan, the "Credit Facility"). Amendment No. 2 revised the covenants related to minimum consolidated EBITDA (as defined in the amended Financing Agreement) for the four consecutive fiscal quarters ending September 30, 2015, December 31, 2015, March 31, 2016 and June 30, 2016 from $22.2 million, $23.1 million, $24.4 million and $25.6 million, respectively, to $14.5 million, $15.0 million, $17.0 million and $17.5 million, respectively. In addition, Amendment No. 2 requires that the Company make additional monthly accelerated principal payments on the Term Loan in the amount of $0.5 million commencing on October 15, 2015 and continuing until the Term Loan has been paid in full. Amendment No. 2 also requires that we make additional accelerated payments at the end of each calendar quarter in the amount of all unrestricted cash on hand as of the close of business on the last day of the quarter in excess of $12.5 million.
The principal amount of the Term Loan is payable in consecutive quarterly installments beginning with the calendar quarter ended March 31, 2014 and matures on the earlier of October 18, 2018 or such date as the outstanding loans become payable in accordance with the terms of the Financing Agreement (the “Final Maturity Date”). The Term Loan bears interest at a rate equal to 7.5% per annum plus the greater of (i) 1.25% or (ii) LIBOR, or at the Company’s option, a reference rate (as defined in the Financing Agreement) plus 6.5% per annum, with such interest payable monthly. For the year ended June 30, 2015 the average interest rate was 8.75%.
The Company’s obligations under the Credit Facility are secured by a security interest in substantially all of the Company’s assets. Loans outstanding under the Credit Facility (1) must be prepaid based on certain cash flow metrics and with any net proceeds of certain permitted asset sales and (2) may be prepaid in whole or in part at any time, with any prepayments made prior to the first anniversary of the effective date subject to a prepayment premium. Any principal amount of the loans which is prepaid or repaid may not be re-borrowed. During the year ended June 30, 20122015, the Company made principal prepayments against the outstanding indebtedness of $4.5 million as part of the Amendment to the Term Loan discussed above.
The Credit Facility contains customary negative covenants that, among other things, restrict the Company from undertaking specified corporate actions such as creation of liens, incurrence of additional indebtedness, making certain investments with affiliates, changes of control, having excess foreign cash, issuance of equity, repurchasing the Company's

F - 14



equity securities, and making certain restricted payments, including dividends, without prior approval from the lender. The Credit Facility also contains various financial covenants that require the Company to maintain a certain consolidated EBITDA, certain leverage and fixed charges ratios as well as a minimum level of liquidity. Additionally, the Credit Facility contains cross-default provisions, whereby a default pursuant to the terms and conditions of certain indebtedness will cause a default on the remaining indebtedness under the Credit Facility. At June 30, 2015, the Company was in compliance with the applicable covenants including those under the amended Credit Facility.
The Company incurred transaction costs associated with the Credit Facility totaling $2.7 million, of which $0.5 million and $0.3 million was recorded in interest expense during the years ended June 30, 2015 and 2014, respectively. The remaining $1.9 million as of June 30, 2015 consists of unamortized deferred debt offering costs and debt discount included in the accompanying consolidated balance sheet and are amortized to interest expense using the interest method.
The Company’s book value for the Credit Facility approximates the fair value. Aggregate future principal payments required in accordance with the terms of the Credit Facility are as follows (in thousands):
Year ending June 30,Amount
2016$11,141
201710,484
 $21,625
Note 7 — Stockholders’ Equity
During the years ended June 30, 2015, 2014, and 2013, the Company issued 11,909,2042.6 million, 5.2 million, and 7.3 million shares, respectively, of common stock as a result of the exercise of options and warrants. In addition,warrants and during the years ended June 30, 2015, 2014, and 2013, the Company issued 149,2531.3 million, 0.2 million, and 2.6 million shares, respectively, of restricted common stock. During the year ended June 30, 2015, 0.9 million shares of restricted stock were canceled or surrendered as payment of tax withholding upon vesting.
On November 6, 2014, the Company announced a share repurchase program authorizing it to repurchase up to $7.0 million in shares of the Company's common stock. As part of that repurchase program, the Company entered into a pre-arranged stock repurchase plan that operated in accordance with guidelines specified under Rule 10b5-1 of the Securities Exchange Act of 1934. The pre-arranged stock repurchase program terminated in accordance with its terms on February 13, 2015. Pursuant to the program, the Company purchased 4.5 million shares of its common stock at an aggregate purchase price of $5.9 million. The remaining $1.1 million authorized under the program for repurchases was unused.
On June 3, 2014, the Company announced a share repurchase program authorizing it to employees

repurchase up to $4.0 million in shares of the Company's common stock. As part of that repurchase program, the Company entered into a pre-arranged stock repurchase plan that operated in accordance with guidelines specified under Rule 10b5-1 of the Securities Exchange Act of 1934. The pre-arranged stock repurchase program terminated in accordance with its terms on December 31, 2014. Pursuant to the program, the Company purchased 3.0 million shares of its common stock at an aggregate purchase price of $4.0 million under this repurchase program.

On March 11, 2014 the Company announced a share repurchase program authorizing it to repurchase up to $3 million of shares of the Company's common stock. As part of that repurchase program, the Company entered into a pre-arranged stock repurchase plan that operated in accordance with guidelines specified under Rule 10b5-1 of the Securities Exchange Act of 1934. The pre-arranged stock repurchase program terminated in accordance with its terms on June 8, 2014. Pursuant to the program, the Company purchased 2.2 million shares of its common stock at an aggregate purchase price of $3 million under this repurchase program.
On November 1, 2013, the Company accepted for payment an aggregate of 16.3 million shares of its common stock at an aggregate purchase price of $40 million as a result of its modified Dutch auction tender offer (the "Tender Offer") that expired October 25, 2013. The Company incurred transaction costs of $0.3 million related to the Tender Offer. The Company entered into the Credit Facility to finance this repurchase. (see Note 6).
On March 22, 2013 the Company announced a share repurchase program authorizing it to repurchase up to $5 million of shares of the Company's common stock. As part of that repurchase program, the Company entered into a pre-arranged stock repurchase plan that operated in accordance with guidelines specified under Rule 10b5-1 of the Securities Exchange Act of 1934. The pre-arranged stock repurchase program terminated in accordance with its terms on December 1, 2013. Pursuant to the program, the Company purchased 2.1 million shares of its common stock at an aggregate purchase price of $5 million under this repurchase program.

F - 15



The Company’s Articles of Incorporation authorize the issuance of preferred shares. However, as of June 30, 2012,2015, none have been issued nor have any rights or preferences been assigned to the preferred shares by the Company’s Board of Directors.

Note 58Stock Option GrantsShare-Based Compensation
Long-Term Incentive Plans
The Company adopted and Warrantsthe shareholders approved the Company’s 2007 Long-Term Incentive Plan (the “2007 Plan”), effective November 21, 2006, to provide incentives to certain employees, directors and consultants. A maximum of 10.0 million shares of the Company’s common stock can be issued under the 2007 Plan in connection with the grant of awards. Awards to purchase common stock have been granted pursuant to the 2007 Plan and are outstanding to various employees, officers, directors, Scientific Advisory Board members and independent distributors at prices between

Stock Option Grants$0.21 and $1.50 per share, with initial vesting periods of one to three years. Awards expire in accordance with the terms of each award and the shares subject to the award are added back to the 2007 Plan upon expiration of the award. The contractual term of stock options granted is generally ten years. As of June 30, 2015 there were awards outstanding, net of awards expired, for the purchase in aggregate of 2.1 million shares of the Company’s common stock.

The Company adopted and the shareholders approved the 2010 Long-Term Incentive Plan (the “2010 Plan”), effective September 27, 2010, as amended on August 21, 2014, to provide incentives to certain employees, directors and consultants who contribute to the strategic and long-term performance objectives and growth of the Company. A maximum of 10.5 million shares of the Company’s common stock can be issued under the 2010 Plan in connection with the grant of awards. Awards to purchase common stock have been granted pursuant to the 2010 Plan and are outstanding to various employees, officers and directors. Outstanding stock options awarded under the 2010 Plan have exercise prices between $0.63 and $3.53 per share, and vest over one to four year vesting periods. Awards expire in accordance with the terms of each award and the shares subject to the award are added back to the 2010 Plan upon expiration of the award. The contractual term of stock options granted is generally ten years. As of June 30, 2015 there were awards outstanding, net of awards expired, for an aggregate of 1.2 million shares of the Company’s common stock.
The Company adopted a Performance Incentive Plan effective July 1, 2013 (the "Fiscal 2014 Performance Plan"). The Fiscal 2014 Performance Plan is intended to provide selected employees an opportunity to earn performance-based cash bonuses whose value is based upon the Company’s stock value and to encourage such employees to provide services to the Company and to attract new individuals with outstanding qualifications. The Fiscal 2014 Performance Plan seeks to achieve this purpose by providing for awards in the form of performance share units (the “Units”). No shares will be issued under the Fiscal 2014 Performance Plan. Awards may be settled only with cash and will be paid subsequent to award vesting. The fair value of share-based compensation awards, that include performance shares, are accounted for as liabilities. Vesting for the Units is subject to achievement of both service-based and performance-based vesting requirements. Performance-based vesting occurs in three installments if the Company meets certain performance criteria generally set for each year of a three-year performance period. The service-based vesting criteria occurs in three annual installments which are achieved at the end of a given fiscal year only if the participant has continuously remained in service from the date of award through the end of that fiscal year. The fair value of these awards is based on the trading price of the Company's common stock and is remeasured at each reporting period date until settlement. The Company adopted a separate Performance Incentive Plan effective July 1, 2014 (the "Fiscal 2015 Performance Plan"). The Fiscal 2015 Performance Plan is substantially similar to the Fiscal 2014 Performance Plan except that the service-based vesting criteria occurs in a single installment and is achieved at the end of the third fiscal year after the award is granted if the participant has continuously remained in service from the date of the award through the end of the third fiscal year.
Stock-Based Compensation
In accordance with accounting guidance on stock basedstock-based compensation, payments in equity instruments for goods or services are accounted for by the fair value method. For the fiscal years ended June 30, 20122015, 2014, and 2011, stock based2013, stock-based compensation of $1,322,566$1.7 million, $2.6 million and $766,485$2.2 million, respectively, was reflected as an increase to additional paid in capital. Ofcapital and $0.1 million and 0.3 million was reflected as an increase to other accrued expenses for the $1,322,566 stock basedfiscal years ended June 30, 2015 and 2014. There were no increases to other accrued expenses related to stock-based compensation for the fiscal year ended June 30, 2012, $1,188,7352013. For the fiscal years ended June 30, 2015, 2014, and 2013, all stock-based compensation was employee related.
At June 30, 2015 there was $2.9 million of unrecognized compensation cost related and $133,831 was non-employee related. Ofto nonvested share-based compensation arrangements under the $766,4852010 Plan, based on management's estimate of the shares that will ultimately vest. The Company expects to recognize such costs over a weighted-average period of 1.9 years.

-F - 16-



Stock Options
The weighted-average grant-date fair value of stock based compensation foroptions granted during the fiscal year ended June 30, 2011, $670,0732013 was employee related and $96,412 was non-employee related.

The Company granted$2.49. There were no stock options to various of its employees, directors and independent distributorsoption grants during the yearfiscal years ended June 30, 2012. 2015 and 2014.

The options grant the right to purchase sharesfair value of the Company’s common stock at prices between $1.33 and $3.53 per share. The Company granted options to purchase shares of the Company’s common stock during the year ended June 30, 2011 at prices between $0.48 and $1.28 per share. The options are not transferable and expire on various dates through June 23, 2021. The Company also granted Stock Appreciation Rights (SARs) to an employee during the year ended June 30, 2012. The intent is to settle the SARs in cash and they are being accounted foroption awards was estimated using the liability method which requires re-measurement at each reporting period.

Black-Scholes option-pricing model with the following assumptions and weighted-average fair values:

 June 30,
 2015 2014 2013
Risk-free interest rateN/A N/A 0.82%
Dividend yieldN/A N/A %
Expected life in yearsN/A N/A 5.0- 6.08
Expected volatilityN/A N/A 127%
The following is a summary of stock option activity for the years ended June 30, 20122015, 2014, and 2011:

   Options  Weighted
Average
Exercise Price
   Weighted
Average Remaining
Contractual Term
 

Outstanding and exercisable, June 30, 2010

   8,535,731   $0.50     8.39  
  

 

 

    

Granted

   2,632,000   $1.04     9.65  

Exercised

   (469,571 $0.32     7.54  

Forfeited

   (200,000 $0.74     —    

Expired or Cancelled

   —     $0.00     —    
  

 

 

    

Outstanding and exercisable, June 30, 2011

   10,498,160   $0.64     7.93  
  

 

 

    

Granted

   2,249,503   $2.00     9.11  

Exercised

   (1,612,000 $0.45     6.97  

Forfeited

   (28,667 $1.57     —    

Expired or Cancelled

   —       
  

 

 

    

Outstanding and exercisable, June 30, 2012

   11,106,996   $0.94     7.36  
  

 

 

    

Warrants2013

At :

 Options (in thousands) 
Weighted
Average
Exercise Price
 
Weighted
Average Remaining
Contractual Term (in years)
 Aggregate Intrinsic Value (in thousands)
Outstanding at June 30, 201210,945
 $0.91
 
 

        
Granted152
 $2.82
 
 

Exercised(3,319) 0.49
 
 $7,128
Forfeited(768) 1.54
 
  
Expired or Canceled
 
 
  
Outstanding at June 30, 20137,010
 1.08
 
 

        
Granted
 $
 
 

Exercised(1,400) 0.69
 
 $2,282
Forfeited(469) 1.84
 
  
Expired or Canceled
 
 
  
Outstanding at June 30, 20145,141
 1.18
 
 

        
Granted
 $
 
 

Exercised(155) 0.72
 
 $60
Forfeited(1,756) 1.31
 
  
Expired or Canceled
 
    
Outstanding at June 30, 20153,230
 1.12
 4.87 $113
Exercisable at June 30, 20153,119
 $1.07
 4.80 $113

F - 17



Restricted Shares
The following is a summary of restricted shares granted during the years ended June 30, 2012, warrants to purchase an aggregate2015, 2014, and 2013:
Nonvested Shares Shares (in thousands) Weighted Average Grant Date Fair Value
Nonvested at June 30, 2012 162
 
     
Granted 2,808
 $2.62
Vested (37) 3.34
Forfeited (196) 3.25
Nonvested at June 30, 2013 2,737
 2.61
Vested at June 30, 2013 
 
     
Granted 225
 $1.79
Vested (760) 2.65
Forfeited (478) 2.55
Nonvested at June 30, 2014 1,724
 2.46
Vested at June 30, 2014 
 
     
Granted 1,325
 $0.8
Vested (531) 2.37
Forfeited (770) 2.22
Nonvested at June 30, 2015 1,748
 1.34
Vested at June 30, 2015 
 
The total vesting date fair value of 12,964,235restricted shares ofthat vested during the Company’s common stock were outstanding. There were no warrants issued duringyears ended June 30,2015, 2014 and 2013 was $0.6 million, $1.2 million and $0.1 million, respectively.
Performance Stock Units
During the year ended June 30, 2012.

At June 30, 2011, warrants2015, the Company awarded performance stock units (the "Performance Stock Units") to purchase an aggregateits executive officers (the "Recipients). Vesting for the Performance Stock Units occurs over three consecutive annual performance periods and is subject to achievement of 25,460,094both service based and market based performance vesting requirements. Subject generally to the Recipient's continued service with the Company (the serviced based requirement), each Performance Stock Unit represents a contingent right for the Recipient to receive, within thirty days after the end of each of three annual performance periods, a distribution of shares of the Company’s common stock were outstanding. There were no warrants issuedof the Company equal to 0% to 200% of the target number of Performance Stock Units subject to the award for each performance period. The actual number of shares distributed will be based on the Company's total stockholder return ("TSR") performance during the relevant performance period, subject to acceleration upon a change in control of the Company. The vesting for 50% of the target Performance Stock Units is based upon the Company's absolute TSR for the Performance Period as compared to a matrix of fixed numeric values and the vesting for the other 50% of the target Performance Stock Units is based upon a relative comparison of the Company's TSR to the Vanguard Russell 2000 exchange traded fund. The weighted average grant date fair value of Performance Stock Units granted during the fiscal year ended June 30, 2011.

2015 was $1.54, which will be recognized on a straight-line basis over the requisite service period, regardless of when, if ever, the market based performance conditions are satisfied. There were no Performance Stock Units granted during the years ended June 30, 2014 and 2013.

The fair value of Performance Stock Units granted was estimated using a Monte Carlo simulation model which included the following assumptions in order to reflect the performance conditions that must be satisfied for the share units to vest:
June 30, 2015
Risk-free interest rate1.07%
Dividend yield%
Expected volatility - company54.1%
Expected volatility - peer company15.7%
Total measurement period (years)3.0

F - 18



The following is a summary of Performance Stock Units granted during the year ended June 30, 2015:
 Number of Units (in thousands) Weighted Average Grant Date Fair Value
Nonvested at June 30, 2014
 
    
Granted1,600
 $1.54
Vested
 
Forfeited(800) 1.54
Nonvested at June 30, 2015800
 1.54
Vested at June 30, 2015
 
Cash-Settled Performance Units
The following is a summary of cash settled performance units granted during the years ended June 30, 2015 and 2014:
 Number of Units (in thousands) Weighted Average Grant Date Fair Value
Outstanding at June 30, 2013, nonvested
 $
Granted245
 1.48
Vested(214) 
Forfeited(31) 1.51
Outstanding at June 30, 2014, nonvested
 
Granted482
 1.15
Vested(353) 
Forfeited(129) 1.16
Outstanding at June 30, 2015, nonvested
 
The fair value of vested awards under the Performance Plan as of June 30, 2015 was $0.2 million. Payments of $0.3 million were made to settle vested cash settled performance units during the year ended June 30, 2015. No payments were made to settle vested cash-settled performance units during the fiscal year ended June 30, 2014. No cash-settled performance units were granted or outstanding during the fiscal year ended June 30, 2013.
Warrants
As of June 30, 2015, the Company had outstanding warrants which were issued in conjunction with convertible debentures between November 2009 and February 2010.

F - 19



The following is a summary of the warrants issuedwarrant activity for the years ended June 30, 20122015, 2014, and 2011:

2013 (in thousands):
 
Common
Stock
Warrants

Outstanding and exercisable, June 30, 2010

38,580,294

Issued

107,992

Cancelled

—  

Exercised

(13,228,192

Expired

—  

Outstanding and exercisable, June 30, 2011

25,460,094

Issued

270,000

Cancelled

—  

Exercised

(12,562,859

Expired

(203,000

Outstanding and exercisable, June 30, 2012

12,964
12,964,235 
Issued


Canceled


Exercised(4,723)
Expired
Outstanding and exercisable at June 30, 20138,241
 
Issued
Canceled
Exercised(3,996)
Expired
Outstanding and exercisable at June 30, 20144,245
Issued
Canceled
Exercised(3,637)
Expired
Outstanding and exercisable at June 30, 2015608

As of June 30, 20122015, 2014, and 2013, the Company had no warrants classified as derivative liabilities.

As

Note 9 — Other Income (Expense), net
Other income (expense), net consists of the following (in thousands):
 Year ended June 30,
 2015 2014 2013
Business development incentive, net$
 $666
 $695
Foreign currency transaction loss, net(498) (194) (1,689)
Gain on settlement of forward contract203
 8
 42
Other income (expense), net136
 (96) 40
  Total other income (expense), net$(159) $384
 $(912)
In January 2013, the Company began operations of a foreign subsidiary that qualified for a government-sponsored business development incentive. Under the incentive program, the Company's foreign subsidiary was allowed to retain certain non-income based taxes during the twelve month period ending December 31, 2013, rather than remit such taxes to the tax authorities. The income associated with the retention of these taxes is included in "Business development incentive, net" in the table above. No such incentives were realized during the fiscal year ended June 30, 2011 the Company classified warrants to acquire an aggregate of 8,360,000 shares issued in conjunction with the 2009 private placement of common stock as a short-term derivative liability. The Company estimated the fair value of the liability at June 30, 2011 as $7,435,883 using the Black-Scholes Merton model adjusted for dilution with the following assumptions:

1)risk free rate of 0.29 percent;

2)dividend yield of -0- percent;

3)expected life of 0.72 to 0.78 years;

4)a volatility factor of the expected market price of the Company’s common stock of 106 percent.

As of June 30, 2011 the Company classified warrants to acquire an aggregate of 15,168,052 shares issued in conjunction with the 2009 and 2010 convertible debentures as a long-term derivative liability. The Company estimated the fair value of the liability at June 30, 2011 as $19,905,401 using the Black-Scholes Merton model adjusted for dilution with the following assumptions:

1)risk free rate of 0.81 to 2.13 percent;

2)dividend yield of -0- percent ;

3)expected life of 3.43 to 5.68 years;

4)a volatility factor of the expected market price of the Company’s common stock of between 137 and 138 percent.

2015.


F - 20



Note 610 — Income Taxes

As of June 30, 2012,2015, the Company had a Federal net operating loss (“NOL”) carry-forward of approximately $5,445,000.$0.4 million. The NOL may be offset against future taxable income, if any, through the year ended net operating losses expire by June 30, 2030. A portion of the NOL carryforward begins to expire in 2024 is and are subject to review by the Internal Revenue Service, and isare subject to U.S. Internal Revenue Code Section 382 limitations. As of June 30, 2015, state NOLs were $8.8 million and foreign NOLs were $0.9 million. The income tax expense (benefit) for the years ended June 30, 20122015, 2014, and 20112013 consists of the following:

   2012  2011 

Income / (Loss) Before Income Taxes:

   

Domestic

  $14,557,000   $(50,534,720

International

   116,000    (165,030
  

 

 

  

 

 

 
  $14,673,000   $(50,699,750
  

 

 

  

 

 

 

Current Taxes

   

Federal

  $3,758,000   $—    

State

   1,121,000    92,000  

Foreign

   47,000    —    
  

 

 

  

 

 

 

Total Current Income Tax Provision

  $4,926,000   $92,000  

Deferred Taxes

   

Federal

   (2,110,000  —    

State

   (602,000  —    

Foreign

   (12,000  —    
  

 

 

  

 

 

 

Total Deferred Income Tax Provision

  $(2,724,000 $—    
  

 

 

  

 

 

 

Net Income Tax Provision

  $2,202,000   $92,000  
  

 

 

  

 

 

 

following (in thousands):

 2015 2014 2013
Income / (Loss) Before Income Taxes:     
Domestic$8,249
 $13,894
 $11,250
International2,404
 2,761
 (97)
 $10,653
 $16,655
 $11,153
Current Taxes:     
Federal$2,600
 $2,010
 $4,087
State446
 72
 383
Foreign856
 1,018
 (33)
Total Current Income Tax Provision$3,902
 $3,100
 $4,437
Deferred Taxes:     
Federal97
 2,299
 (706)
State4
 83
 (77)
Foreign(337) (210) (109)
Total Deferred Income Tax Provision$(236) $2,172
 $(892)
Net Income Tax Provision$3,666
 $5,272
 $3,545
The effective income tax rate for the years ended June 30, 20122015, 2014, and 20112013 differs from the U.S. Federal statutory income tax rate due to the following:

   2012  2011 

Federal statutory income tax rate

   35.00  (34.00%) 

State income taxes, net of federal benefit

   5.50  .24

Tax return to provision true-up

   (1.01)%   (1.35%) 

Permanent differences:

   

— interest on convertible debt

   0.00  3.44

— change in derivative liability

   16.14  32.44

— stock option compensation

   0.30  .21

— other

   0.44  0.12

Decrease in valuation allowance

   (39.45)%   (0.91%) 
  

 

 

  

 

 

 

Net income tax provision (benefit)

   16.04  (0.18%) 
  

 

 

  

 

 

 

 2015 2014 2013
Federal statutory income tax rate35.0 % 35.0 % 35.0 %
State income taxes, net of federal benefit2.0 % 1.9 % 1.8 %
Tax return to provision true-up1.2 % (3.0)% (2.5)%
Permanent differences:     
— stock based compensation1.2 % 1.3 % 0.8 %
       — domestic production activities deduction(1.6)% (1.8)% (2.7)%
       — credit for increasing research activities(3.8)% (1.5)% (0.7)%
— other0.4 % (0.5)% 0.0 %
Change in valuation allowance0.0 % 0.1 % 0.0 %
Net income tax provision34.4 % 31.5 % 31.7 %

F - 21



The components of the deferred tax assets and liabilities as of June 30, 20122015 and 20112014 are as follows:

   2012  2011 

Deferred tax assets:

   

Federal and state net operating loss carryovers

  $2,453,000   $4,832,000  

Research and development tax credits

   —      31,000  

Contribution carryover

   —      13,000  

Stock option compensation

   988,000    722,000  

Accrued vacation, allowance for returns, bonuses & other

   600,000    540,000  
  

 

 

  

 

 

 

Deferred tax asset

  $4,041,000   $6,138,000  

Deferred liabilities

   

Patents and trademarks

   (587,000  (625,000

Change in tax accounting methods

   (44,000  (36,000

Property & equipment

   (540,000  (6,000
  

 

 

  

 

 

 

Total deferred liabilities

   (1,171,000  (667,000
  

 

 

  

 

 

 

Net deferred tax asset

   2,870,000    5,471,000  

Less: valuation allowance

   (147,000  (5,471,000
  

 

 

  

 

 

 

Deferred tax assets

  $2,723,000   $—    
  

 

 

  

 

 

 

follows (in thousands):

 2015 2014
Deferred tax assets:   
Federal, state, and foreign net operating loss carryovers$656
 $1,016
Stock option compensation1,353
 1,353
Accrued vacation, allowance for returns, bonuses & other1,395
 572
Gross deferred tax asset$3,404
 $2,941
    
Deferred tax liabilities:   
Patents and trademarks(468) (500)
Change in tax accounting methods(98) (198)
Property & equipment(1,268) (583)
Gross deferred tax liabilities(1,834) (1,281)
Less: valuation allowance(218) (217)
Deferred tax assets, net$1,352
 $1,443
The Company has adopted accounting guidance for uncertain tax positions which provides that in order to recognize an uncertain tax benefit, the taxpayer must be more likely than not of sustaining the position, and the measurement of the benefit is calculated as the largest amount that is more than 50% likely to be realized upon recognition of the benefit. We believe the Company has no material uncertain tax positions and do not expect significant changes within the next twelve months in the amount of unrecognized tax benefits that may occur within the next twelve months.benefits. Accordingly, we have not reserved for interest or penalties. The tax years open for examination by the Internal Revenue Service (“IRS”) include returns for fiscal years June 30, 20092012 through present and the open tax years by state tax authorities include returns for fiscal years June 30, 20082010 through present. In addition, the IRS and state tax authorities may examine NOLs for any previous years if utilized by the Company.

The total recognizedCompany conducts its business globally. As a result, the Company and its subsidiaries file income tax benefit from settlement of stock based awardsreturns in the U.S. federal jurisdiction and various state and foreign jurisdictions, and are subject to examination for the period ending open tax years of June 30, 2011 was $579,000.

2010Note 7 — Related Parties through

During the year ended June 30, 2012 one of the Company’s board members earned2014.

Note 11 — Commitments and was paid $30,605Contingencies
Operating Leases
The Company leases its facilities under a consulting agreementnon-cancelable operating leases, which was terminated in January of 2012 in conjunction with expiration of that board member’s term of service as a director.

During the year ended expire at various dates through 2024. The facilities leases contain renewal options and are subject to cost increases. Future minimum annual payments under non-cancelable operating leases at June 30, 2011 one of2015 are as follows (in thousands):

Year ending June 30,Amount
2016$2,427
20172,439
20181,328
20191,246
20201,290
Thereafter5,105
Total future minimum lease payments$13,835
Rent expense totaled $2.4 million, $1.9 million, and $1.8 million for the Company’s board members earned and was paid $30,546 under a consulting agreement. Also during the yearyears ended June 30, 20112015, 2014, and 2013, respectively. In addition, the daughterCompany has $0.2 million of a board member was paid $11,000 andsublease income to be received product in exchange for promotional activities.

Duringthrough the year ended June 30, 2011 oneend of the Company’s board members earned $443,410 under a consulting agreement. fiscal 2016.

Contingencies
The Company paidis occasionally involved in lawsuits and disputes arising in the board member $388,935 duringnormal course of business. The Company regularly reviews all pending litigation matters in which it is involved and establishes accruals deemed appropriate by management for these litigation matters when a probable loss estimate can be made. In the year andopinion of management, the amounts accrued for as of June 30, 2011 owed2015 are appropriate based on the remaining $54,475 which was subsequently paid in July 2012.

During the year ended June 30, 2011 a board member converted a debenture with a face valueprobable outcome of $499,500 into 2,497,500 shares of the Company’s common stock. The debenture was issued as a conversion from a bridge

loan as follows: during the year ended June 30, 2010 one of the Company’s investors made a bridge loan to the Company for $500,000 at 3% per month interest. Subsequent to making the loan the investor became a board member and the principal was converted to convertible debt as part of and under the same terms as the debenture issuance which closed in February 2010. The accrued interest was repaid in cash at that time.

currently pending matters.


F - 22



Note 8 — Commitments

Corporate Offices

On July 31, 2008 the Company entered into a five (5) year lease agreement in San Diego, California. Pursuant to the lease agreement, we prepaid rent of $7,850. Monthly rent payments began July 1, 2008 and are as follows: $7,850 for July 2008; rent is abated during the months of August, September and October 2008, $7,850 per month from November 2008 through June 2009; $8,125 per month from July 2009 through June 2010; $8,409 per month from July 2010 through June 2011; $8,703 per month from July 2011 through June 2012; and $9,008 per month from July 2012 through June 2013.

In March 2009 the Company entered into a thirty nine (39) month sublease in South Jordan, Utah. Pursuant to the agreement, we prepaid rent of $17,256. Monthly rent payments of $17,256 began March 1, 2009 and are as follows: $17,256 per month from March 2009 through February 2010; $17,773 per month from March 2010 through February 2011; $18,306 per month from March 2011 through February 2012; and $18,855 per month from March 2012 through May 31, 2012. As of April 2012, the Company was allowed to terminate the lease early in exchange for some existing leasehold improvements with a net book value of less than $30,000.

In September 2011 the Company entered into a sixty six (66) month lease agreement in Sandy, Utah. Pursuant to the lease agreement, we prepaid rent of $35,748. In June 2012 the lease was amended to add additional space. Monthly rent payments are as follows: $35,748 per month from July 2012 to August 2012;$44,645 per month from September 2012 through June 2013; $45,538 per month from July 2013 through June 2014; $46,449 per month from July 2014 through June 2015; $47,378 per month from July 2015 through June 2016; and $48,326 per month from July 2016 through June 2017.

Rent expense totaled $408,764 and $319,070 for the years ended June 30, 2012 and 2011, respectively.

As of June 30, 2012, future minimum lease payments under the non-cancelable leases are as follows:

Year ending June 30,

  

2013

  $626,042  

2014

   546,459  

2015

   557,388  

2016

   568,536  

2017

   579,910  
  

 

 

 

Total future minimum Lease payments

  $2,878,335  
  

 

 

 

Other Commitments

   Payments due by period 

Contractual Obligations

  Total   Less than
1 year
   1-3 years   3-5 years 

Operating Lease Obligations

  $2,878,335    $626,042    $1,672,383    $579,910  

Note 912 — Interim Financial Results (Unaudited)

The following summarizes selected quarterly financial information for quarterly periods during the years ended June 30, 20122015 and 2011:

2014:

LIFEVANTAGE CORPORATION AND SUBSIDIARY

SUBSIDIARIES

CONDENSED CONSOLIDATED QUARTERLY RESULTS

(in ‘000’sthousands except per share data)

   Quarter   Year
ended
June 30, 2012
 

Year ended June 30, 2012

  First   Second   Third  Fourth   

Sales, net

  $20,083    $25,284    $36,212   $44,604    $126,183  

Gross profit

   17,127     21,604     31,223    38,177     108,131  

Net income (loss)

  $3,724    $8,759    $(4,846 $4,832    $12,469  

Per common share:

         

Income (loss) per share, basic

  $0.04    $0.09    $(0.05 $0.04    $0.12  

Income (loss) per share diluted

  $0.02    $0.05    $(0.05 $0.04    $0.11  

    Quarter  Year
ended
June 30, 2011
 

Year ended June 30, 2011

  First  Second  Third  Fourth  

Sales, net

  $6,443   $7,460   $9,975   $15,041   $38,919  

Gross profit

   5,423    6,269    8,393    12,917   $33,002  

Net income (loss)

  $715   $5,448   $(9,768 $(47,187 $(50,792

Per common share:

      

Income (loss) per share, basic

  $0.01   $0.08   $(0.13 $(0.56 $(0.69

Income (loss) per share, diluted

  $(0.01 $(0.00 $(0.13 $(0.56 $(0.69

 Fiscal Quarter Year ended June 30, 2015
 First Second Third Fourth 
Revenue, net$51,633
 $48,247
 $45,155
 $45,301
 $190,336
Gross profit45,954
 40,761
 37,603
 38,008
 162,326
Net income$4,716
 $1,472
 $573
 $226
 $6,987
Per common share:         
Income per share, basic$0.05
 $0.02
 $0.01
 $
 $0.07
Income per share, diluted$0.05
 $0.01
 $0.01
 $
 $0.07
 Fiscal Quarter Year ended June 30, 2014
 First Second Third Fourth 
Revenue, net$51,328
 $51,538
 $55,064
 $56,038
 $213,968
Gross profit43,519
 43,594
 46,605
 47,056
 180,774
Net income$3,256
 $3,282
 $2,494
 $2,351
 $11,383
Per common share:         
Income per share, basic$0.03
 $0.03
 $0.02
 $0.02
 $0.11
Income per share, diluted$0.03
 $0.03
 $0.02
 $0.02
 $0.10
Note 1013 — Subsequent Events

On July 2, 2012, Lifevantage Japan KK,2015 the Company announced that it terminated the employment of David Colbert as lessee, entered into a fixed term building leaseChief Financial Officer, effective July 3, 2015. Pursuant to Mr. Colbert's employment agreement, with Gashu Enterprise KK, as lessor, for office space locatedhe will receive severance in Tokyo, Japan. The term of the lease is for five years commencing on August 1, 2012 and the monthly rent is approximately $108,000 (at the current foreign currency exchange rate and including common area charges and applicable taxes). If the lessor terminates the lease due to our breach of its terms or for other specified reasons, we must pay the lessor an aggregate amount equal to $325,000 to be paid in substantially equal monthly installments over the rent that would have been payable for12 month period following the termtermination date.
On July 15, 2015 the Company terminated the employment of David Phelps as Chief Sales Officer. Pursuant to Mr. Phelps' employment agreement, he will receive severance in an aggregate amount equal to $352,000 to be paid in substantially equal monthly installments over the lease. At such time as12 month period following the lease agreement terminates or expires and we vacate the building, we are required to return the leased area to its original state at our cost.

We formed a wholly-owned subsidiary, LifeVantage Canada Ltd., under the Companies Act (Nova Scotia) on July 30, 2012.

The USPTO issued Patent No. 8,221,805 to us on July 17, 2012, which patent resulted from U.S. Patent Application No. 13/039,073, Compositions for Alleviating Inflammation and Oxidative Stress in a Mammal.

F-21

termination date.

F - 23