Dr. Fitt Intelligent Designs, LLC
November 7, 2018
Roby D. Mitchell
Dr. Fitt Intelligent Designs, LLC
812 S Georgia St
Amarillo, TX 79106
9818 Plum Creek Dr.
Amarillo, TX 79124
RE: BALI Greens, BALI Purples, Black Seed Oil, DHEA Capsules, Lugol’s Solution 2% Drops, Robenyzme Capsules, OMG Max Drops, New Dawn Capsules, Vitamin C with R-Lipoic Acid
Dear Mr. Mitchell:
This letter is to advise you that the U.S. Food and Drug Administration (FDA) reviewed your websites at www.drfitt.com and www.drfittinfo.com in October 2018 and have found that you take orders there for BALI Greens, BALI Purples, Black Seed Oil, DHEA Capsules, Lugol’s Solution 2% Drops, Robenyzme Capsules, OMG Max Drop, New Dawn Capsules, and Vitamin C with R-Lipoic Acid. FDA also reviewed your Facebook pages, https://www.facebook.com/DrFitt which contains links to your website at www.drfitt.com and https://www.facebook.com/IntelligentDesignAmarillo which contains links to your websites at www.drfitt.com and www.drfittinfo.com. Various claims and statements made on your websites and/or in other labeling establish that these products are drugs as defined in 21 U.S.C. § 321(g)(1)(B) because they are intended for the treatment, cure, mitigation, or prevention of disease. For example, your websites recommend or suggest the use of BALI Greens, BALI Purples, Black Seed Oil, DHEA Capsules, Lugol’s Solution 2% Drops, Robenyzme Capsules, OMG Max Drops, New Dawn Capsules, and Vitamin C with R-Lipoic Acid to treat, cure, mitigate or prevent Alzheimer’s disease, asthma, cancer, cardiovascular diseases, HIV, hypercholesterolemia, hypertension, MRSA, diabetes, dementia, pneumonia, depression and influenza. As explained further below, the introduction of these products into interstate commerce for such uses violates the Federal Food, Drug, and Cosmetic Act.
These products are also new drugs as defined under 21 U.S.C. § 321(p) because they are not generally recognized as safe and effective for the uses recommended or suggested in their labeling. Before a new drug may be marketed or otherwise introduced into interstate commerce, it must be approved by FDA on the basis of scientific data demonstrating that the drug is safe and effective under the conditions of use in its labeling. See 21 U.S.C. §§ 355(a) and 331(d). Your drug products do not have FDA-approved applications as required by 21 U.S.C. § 355.
We advise you to review all materials through which you communicate to consumers the intended uses of your products, and to either submit a new drug application (NDA) for products intended for use in treating, curing, mitigating, diagnosing, or preventing a disease or, alternatively, remove all statements indicating that your product are intended for such uses. This would include reviewing your websites, product labels, catalogs, brochures, flyers, package inserts, audio and video, e-commerce and social media accounts you operate (e.g., Amazon, eBay, Facebook and Twitter accounts), as well as any other promotional materials, and removing product claims, consumer testimonials, metatags, and anything else that states or implies that your products are useful in treating, curing, mitigating, diagnosing, or preventing diseases.
For more information on the types of claims that can be used for conventional foods and dietary supplements, please see:
- 21 CFR 101.93
Within 30 calendar days of the date of this letter, please correct the violations described in this letter and notify FDA, via electronic mail at FDAadvisory@fda.hhs.gov, that the violations have been corrected. Include the Online Advisory Letter Reference number (located in the upper right portion of this letter) in all your communications to FDA regarding this matter.
After 30 days from the date of this letter, if your website or other labeling continue to demonstrate that your products are intended to treat, cure, mitigate, or prevent diseases, the name of your firm and this letter will be posted on the FDA webpage for unapproved new drugs illegally marketed for serious diseases.
This letter is not intended to be an all-inclusive review of your website(s) or a list of all violations of law that exist in connection with your products, your website(s) and other product labeling, or at your facilities. FDA expects you to take the necessary steps to ensure that all your products comply with the laws and regulations enforced by FDA.
Health Fraud Branch
U.S. Food and Drug Administration