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WARNING LETTER
•US Chem Labs•February 13, 2024

FDA WARNING_LETTER - US Chem Labs - February 13, 2024

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Record Details

On February 7, 2024, the FDA issued a Warning Letter to US Chem Labs following an October 2023 review of their website, www.uschemlabs.com. The FDA observed the sale of "Semaglutide," "Tirzepatide," and "Thymalin" products, which are marketed as "research chemicals only" but are deemed intended for human use based on website claims.

The products are cited as unapproved new drugs, violating sections 505(a) and 301(d) of the FD&C Act (21 U.S.C. 355(a) and 301(d)), as no approved applications are in effect. Specific concern was raised regarding "Thymalin" being marketed for children without FDA evaluation for safety, effectiveness, and quality.

Furthermore, the products are misbranded under section 502(f)(1) of the FD&C Act (21 U.S.C. 352(f)(1)) because their labeling lacks adequate directions for use by a layperson. As prescription drugs, they require professional supervision. The introduction of these misbranded drugs into interstate commerce violates section 301(a) of the FD&C Act (21 U.S.C. 331(a)).

US Chem Labs must respond in writing within 15

Company
US Chem Labs
Inspection Date
February 13, 2024
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Tina Smith (Director)
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ID · 2d610114-5e26-4046-9892-61c474d9b4fb

Violation Codes10
21.U.S.C. 355(a)21 U.S.C. 331(d)21 U.S.C. 301(d)21 U.S.C. 352(f)(1)21 CFR 201.521 U.S.C. 353(b)(1)(A)21 U.S.C. 321(g)(1)21 U.S.C. 321(p)FD&C Act 505(a)FD&C Act 301(d)

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