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WARNING LETTER
•Glenn Burkett Naples Corporation•February 15, 2022

Glenn Burkett Naples Corporation – FDA Warning Letter, Feb 15, 2022

Record Details

The FDA issued a Warning Letter to Glenn Burkett Wellness after reviewing their websites (glennburkettwellness.com, gb1com.com) and social media (facebook.com/GlennBurkettBeautyFitnessHealth/) in November 2021. The FDA determined that products such as Colloidal Silver 1400 ppm Dropper, Colloidal Silver 1400 Spray, Silver 750 Sinus Spray, Silver Eye Drops, and various kits (Candida, Cardiovascular, Diabetes) are unapproved new drugs and misbranded under the Federal Food, Drug, and Cosmetic Act.

The claims made on the websites and social media, including "Anti-Bacterial, Anti-Fungal, Anti-Viral," and intentions to treat conditions like heartburn, inflammation, depression, and diabetes, establish these products as drugs. Specifically, several colloidal silver products were cited for claims related to mitigating, preventing, treating, diagnosing, or curing COVID-19. The Colloidal Silver 1400 ppm Dropper was also cited for intended use in animals.

These products are considered "new drugs" because they are not generally recognized as safe and effective for their intended uses and lack FDA approval. They are also misbranded because they fail to bear adequate directions for use by a layperson, as they are intended for conditions requiring professional supervision. OTC colloidal silver products are explicitly deemed not GRASE by FDA regulations (21 CFR 31

Company
Glenn Burkett Naples Corporation
Inspection date
February 15, 2022
Product type
Food
Office
Office of Human and Animal Food Operations East Division IV
People
  • Ramon A. Hernandez (Program Director)
  • Pearl Lopina
View Company Profile

ID · 92936bf9-9b5c-4dd0-95fb-b430b46d328d

Violation Codes10
21 U.S.C. 321(g)(1)(B)21 U.S.C. 321(g)(1)(C)21 U.S.C. 321(p)21 U.S.C. 331(d)21.U.S.C. 355(a)21 U.S.C. 352(f)(1)21 U.S.C. 360b(a)21 U.S.C. 351(a)(5)21 CFR 201.521 CFR 310.548

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