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

Public Health Service
Food and Drug Administration
Southwest Region
Denver District Office

 

Bldg 20-Denver Federal Ctr
PO Box 25087
6th Ave & Kipling St
Denver, CO 80225-0087
Telephone: 303-236-3000
FAX: 303-236-3100

April 26, 2002
WARNING LETTER
VIA CERTIFIED MAIL, RETURN RECEIPT REQUESTED

D Gary Young
Managing Director/Owner
Aromatic Research & Technology, LLC
d/b/a Young Living Essential Oils
250 S Main St
Payson, UT 84651

Ref. No. DEN-02- 12

Dear Mr Young:

During an inspection of your facility on the dates of January 30 and February 26, 2002, a Food and Drug Administration (FDA) investigator documented violations of the Federal Food, Drug, and Cosmetic Act (the Act). Your Stevia Extract and Stevia Select products labeled as Dietary Supplements are actively promoted as conventional foods through labeling, including promotional literature and your web site, www.youngliving.com. When used as an ingredient of a conventional food, or when offered and intended for such use, stevia is considered a food additive. Therefore, stevia is an unapproved food additive that is unsafe within the meaning of Section 409 of the Act. The presence of stevia in your products renders them adulterated within the meaning of Section 402(a)(2)(C) of the Act.

Labeling your stevia products as Dietary Supplements does not necessarily make the products dietary supplements as provided for under the Act. Under the Dietary Supplement Health and Education Act of 1994, the definition of a dietary supplement does not include products represented for use as conventional foods [Section 201(ff)(2)(B) of the Act].

Examples of claims that promote your stevia products as conventional foods include:

This letter is not intended to be an all-inclusive review of all labeling and products your firm markets. It is your responsibility to ensure that all products marketed by your firm are in compliance with the Act and its implementing regulations.

We request that you take prompt action to correct these violations. Failure to promptly correct violations may result in enforcement action being initiated by the Food and Drug Administration without further notice. The Federal Food, Drug, and Cosmetic Act provides for the seizure of illegal products and for an injunction against the manufacturer and/or distributor of illegal products.

Please notify this office in writing within fifteen (15) working days of receipt of this letter as to the specific steps you have taken to correct the stated violations. You should also include an explanation of each step being taken to identify and make corrections to assure that similar violations will not recur. If corrective action cannot be completed within 15 working days, state the reason for the delay and the time within which the corrections will be implemented.

Your reply should be sent to the attention of H. Tom Warwick, Compliance Officer, at the above letterhead address.

Sincerely,
/s/
Tyler H. Thornburg
Acting Director

This page was posted on August 20, 2006.

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