Department of Health and Human Services' logo Department of Health and Human Services

Public Health Service
Food and Drug Administration
  Detroit District
300 River Place
Suite 5900
Detroit, MI 48207
Telephone: 313-393-8100
FAX: 313-393-8139


June 3, 2008

Robert Cloutier
Nu-Gen Nutrition, Inc.
Vitasalus. Inc.
Equinox Products, LLC
1301 Rankin Dr
Troy, MI 48083


Dear Mr. Cloutier:

This is to advise you that the Food and Drug Administration (FDA) has reviewed your websites at the Internet addresses,,,, and and has determined that the products "Ocean Treasure Coral Calcium,""Colostrum," "Electrolyte Formula (Cantron)," "Ellagenol," "Squalamax," "Ultramarine Omega-3TM Virgin Salmon Oil Gelcaps" and "Ultramarine Shark Liver Oil" are promoted for conditions that cause the products to be drugs under section 201(g)(1)(B) of the Federal Food, Drug, and Cosmetic Act (the Act) [21 U.S.C. § 321(g)(1)(B)]. The therapeutic claims on your website establish that the products are drugs because they are intended for use in the cure, mitigation; treatment, or prevention of disease. The marketing of these products with these claims violates the Act.

Examples of some of the claims observed on your websites include:


Further, the "References" section of the Colostrum page of your website cites a number of articles about studies of your Colostrum products or their ingredients. These articles concern the use of the products or their ingredients for treatment or prevention of diseases. When scientific publications are used commercially by the seller of a product to promote the product to consumers, such publications may become evidence of the product's intended use. For example, under 21 CFR 101.93(g)(2)(iv)(C), a citation of a publication or reference in the labeling of a product is considered a claim about disease treatment or prevention if the citation refers to a disease use, and if, in the context of the labeling as a whole, the citation implies treatment or prevention of a disease.

The following are examples of reference citations used to market Colostrum for disease treatment and prevention on your website:


Electrolyte formula (Cantron)

An example of a claim observed on your websites in the form of a testimonial is:


Ultramarine Omega-3™ Virgin Salmon Oil Gelcaps

Ultramarine Shark Liver Oil

In addition, your websites and use a description of the book Shark Liver Oil: Nature's Ainazing Healer, which you also sell, to promote Ultramarine Shark Liver Oil for treatment of cancer. Both Ultramarine Shark Liver Oil and the book are described and offered for sale adjacently on your and websites. Clicking, the "Order" icon on the page takes customers to another page where they can order both the shark liver oil product and the book. which describes the purported efficacy of shark liver oil as a treatment for cancer and other diseases. Clicking on one of the links for your Ultramarine Shark Liver Oil products on your website takes customers to another page where they can order the shark liver oil product and the book, which is listed under "Related Item(s). "The description of the book on your webpages is clearly intended to describe the intended use of Ultramarine Shark Liver Oil. For example, the description of the book on your webpage says that it is "[f]illed with documented studies and remarkable case histories--including testimonials from ... cancer patients whose lives were literally transformed through the use of Shark Liver Oil treatments..." Because of the manner in which Ultramarine Shark Liver Oil and the book are co-promoted on your websites, the book is evidence of the product's intended use as a cancer treatment drug and is considered labeling for the product. See 21 U.S.C. § 321(m); Kordel v. United States, 335 U.S. 345 (1948).

Ocean Treasure Coral Calcium

The claims quoted above are supplemented by the metatags used to bring consumers to your websites through Internet searches. The metatags include "cancer markers," "uterine cancer," "ovarian cancer," and "pancreatic cancer."

Your products are not generally recognized as safe and effective for the above referenced conditions and therefore, the products are "new drttgs" under section 201(p) of the Act [21 U.S.C. § 321(p)]. New drugs may not be legally marketed in the U.S. without prior approval from FDA as described in section 505(a) of the Act [21 U.S.C. § 355(a)]. FDA approves a new drug on the basis of scientific data submitted by a drug sponsor to demonstrate that the drug is safe and effective. Your products "Ocean Treasure Coral Calcium," "Colostrum," "Electrolyte Formula (Cantron)," "Ellagenol," "Squalamax," "Ultramarine Omega-3 TM Virgin Salmon Oil Gelcaps" and "Ultramarine Shark Liver Oil" are also misbranded within the meaning of section 502(f)(1) of the Act, in that labeling for these drugs fail to bear adequate directions for use [21 U.S.C. § 352(f)(1)].

The above violations are not meant to be an all-inclusive list of deficiencies in your products and their labeling. While reviewing your websites, we noticed that you were promoting other products for disease treatment and/or prevention. It is your responsibility to ensure that products marketed by your firm comply with the Act and its implementing regulations. We advise you to review your webs-ites, product labels, and other labeling and promotional materials for your products to ensure that the claims you make for your products do not cause them to violate the Act.

You should take prompt action to correct the violations described above and prevent their future recurrence. Failure to do so may result in enforcement action without further notice.

The Act authorizes the seizure of illegal products and injunctions against manufacturers and distributors of those products [21 §§ U.S.C. 332 and 334].

Please notify this office, in writing, within fifteen (15) working of the receipt of this letter, as to the specific steps you have taken to correct the violations noted above and to assure that similar violations do not occur. Include any documentation necessary to show that correction has been achieved. If corrective actions cannot be completed within fifteen working days, state the reason for the delay and the time within which the corrections will be completed.

Your response should be directed to Judith A. Putz, Compliance Officer at the address above.



Joann M. Givens
District Director
Detroit District Office

This page was posted on July 19, 2010.

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