Inspections, Compliance, Enforcement, and Criminal Investigations
NatureMost of New England 09-Aug-02
Food and Drug Administration
New England District
One Montvale Avenue
Stoneham, Massachusetts 02180
FAX: (781) 596-7896
August 9, 2002
RETURN RECEIPT REQUESTED
Mr. Robert J. Trigo, President
NatureMost of New England, Inc.
dba NatureMost Laboratories, Inc. and Trigo Laboratories, Inc.
60 Trigo Drive
Middletown, CT 06457
Dear Mr. Trigo,
The U.S. Food and Drug Administration (FDA) conducted an inspection of your firm, NatureMost of New England, Inc. (doing business as NatureMost Laboratories, Inc. and Trigo Laboratories, Inc.) located at 60 Trigo Drive, Middletown, CT on June 3 and 6, 2002. Labeling for your firm?s product Calm Focus was collected during the inspection and a review of that labeling indicates serious violations of the Federal Food, Drug land Cosmetic Act (the Act). You can find the Act along with the food, drug and dietary supplement labeling regulations on the Internet through links on FDA?s web page www.fda.gov.
The following violations were noted:
The promotional brochure titled "Trigo Laborafories Calm Focus" states ". . . help children with attention deficit hyperactivity disorder (ADHD)." "Taurine...is used to treat hyperactivity.. ."GABA is effective in treating ADD." "Lecithin - protects against cardiovascular disease.. ." "Passion Flower.. .insomnia and stress related disorders." "Rosemary - fights bacteria.. ." "Ginkgo Biloba.. .good for depression.. ." "Grape Seed.. .moderate allergic and inflammatory responses.. ." These statements cause your product to be a drug as defined in Section 201(g)(l)(B) of the Act. Because we are unaware of any evidence that this product is generally recognized as safe and effective when used as labeled, it also is a new drug under Section 201(p) of the Act.
Under Section 505 of the Act, a new drug may not be legally marketed in the United States without an approved New Drug Application. The product is further misbranded under Section 502(f)(l) of the Act, in that it fails to bear adequate directions for use, and under Section 502(a) of the Act, in that the labeling is false and misleading because it suggests that the product is safe and effective for its intended use. Neither safety nor effectiveness has been established.
Even if this product was not a drug and was to be deemed a dietary supplement, it would violate other provisions of the Act.
Specifically, the product label for "Natural Calm Focus A.D.H.D. (ATTENTION DEFICIT HYPERACTIVITY DISORDER)" states "Calm Focus is a natural approach to help A.D.H.D." These claims are false and misleading in that they are not supported by sufficient scientific studies and therefore they cause your product to be misbranded under Section 403(a)(l) of the Act.
This letter is not intended to be an all-inclusive list of the deficiencies in your product and its labeling. It is your responsibility to ensure that all products marketed by your firm are in compliance with the Act and its implementing regulations. You should review the labeling for all of your products to assure that they are in compliance. We may take further action if you do not promptly correct these violations. For instance, we may seize your products and/or enjoin your firm from operating.
You should notify this office, within fifteen (15) working days of the receipt of this letter, of the specific steps you have taken to correct the noted violations. Copies of the revised labeling should also be submitted. If corrective action cannot be completed within 15 working days, state the reason(s) for delay and the time at which ,the corrections will be completed.
You should direct your reply to Patricia Murphy, Compliance Officer at One Montvale Avenue, Suite 4, Stoneham, MA 02180. If you have any questions concerning this letter, please contact Ms. Murphy at 781-596-7758.
Gail T. Costello
New England District