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WARNING LETTER
•Iotech International, LLC•March 9, 2022

Iotech International, LLC – FDA Warning Letter, Mar 9, 2022

Record Details

On March 15, 2022, the FDA and FTC issued a Warning Letter to Iotech International for selling "ioRinse" and "ioCleanse Molecular iodine Hand Cleanser" on their website and social media, claiming they mitigate, prevent, treat, diagnose, or cure COVID-19. The FDA determined these products are unapproved new drugs under section 505(a) and misbranded drugs under section 502(ee) of the FD&C Act, violating sections 301(a) and (d).

The products are considered "new drugs" because they are not generally recognized as safe and effective (GRASE) for their intended uses, and no FDA-approved applications exist. They do not conform to OTC drug monographs or section 505G requirements for marketing without approval, as their COVID-19 claims exceed general antiseptic uses. "ioCleanse" also contains molecular iodine, an active ingredient not classified in the 1994 TFM.

Iotech International must immediately cease selling these unapproved and unauthorized COVID-19 products. Within 48 hours, they must email COVID-19-Task-Force-CDER@fda.hhs.gov detailing corrective actions and documentation, and email rcleland@ftc.gov certifying cessation of unsubstantiated claims. Failure to comply may result in legal action, including seizure, injunction, civil penalties up to

Company
Iotech International, LLC
Inspection date
March 9, 2022
Product type
Drugs
Office
Center for Drug Evaluation and Research
People
  • Donald D. Ashley (Director)
  • Serena Viswanathan (Associate Director)
View Company Profile

ID · c779828e-2cfb-43f4-a505-255f5aaf378c

Violation Codes10
21.U.S.C. 355(a)21 U.S.C. 352(ee)21 U.S.C. 331(d)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. 35521 U.S.C. 355hFD&C Act 505(a)FD&C Act 501(a)(2)(B)

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