Bliv Wellness LLC dba Bliv
FDA issued a warning letter to Bliv Wellness LLC dba Bliv (Ogden, UT) on February 20, 2026, after reviewing the company's website in December 2025 and finding that it offered compounded semaglutide and tirzepatide products with the 'Bliv' name on the pictured product labels, falsely implying Bliv is the compounder of those drugs when it is not. This constitutes misbranding under FDCA sections 502(a) and 502(bb), and the introduction of these misbranded products into interstate commerce violates section 301(a). FDA required a written response within 15 working days describing corrective steps, and warned that failure to adequately address violations may result in seizure or injunction.
Flagged claims (2)
the representations on your website that Bliv is the compounder of these drug products are false or misleading
The compounded semaglutide and tirzepatide products displayed on your website identify "Bliv" on the pictured label, suggesting Bliv is the compounder of those drugs when in fact it is not.
Required actions (5)
Within fifteen (15) working days of receipt of this letter, please provide a written response to the Office of Compounding Quality and Compliance (OCQC) within the Center for Drug Evaluation and Research (CDER)'s Office of Compliance describing the specific steps you have taken to address any violations.
Addressing the basis for other website claims that could be construed as false or misleading or demonstrating that such claims have been modified or removed in light of FDCA §§ 502(a) and 502(bb)) [21 U.S.C. §§ 352(a) and (bb)].
Identifying the entities that produce the compounded products offered on your website;
Providing a representative sample of labeling for such products;
Failure to adequately address any violations may result in legal action without further notice, including, without limitation, seizure and injunction.
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