PriceTracker GLP-1

What FDA’s record states

FDA record for the warning letter to Lovega LLC dba Pink Pony Peptides
FieldWhat FDA’s record statesSource
RecipientLovega LLC dba Pink Pony PeptidesFDA letter
LocationWellington, FLFDA letter
Letter dateMar 31, 2026FDA letter
Posted by FDAApr 7, 2026FDA index
Issuing officeCenter for Drug Evaluation and Research (CDER)FDA letter
SubjectUnapproved New Drugs Sold Over the InternetFDA letter
MARCS-CMS number721088FDA letter
GLP-1 drugs namedTirzepatide, RetatrutideFDA letter
Response letterNot published by FDAFDA letter
Closeout letterNot published by FDAFDA letter
“Examples from your product labeling, including on your website, that provide evidence of the intended use (as defined in 21 CFR 201.128) of these products as drugs include, but may not be limited to, the following: GLP-2 TZ On the webpage https://pinkponypeptides.com/product/glp2/: “As a dual GIP and GLP-1 receptor agonist, Tirzepatide helps: o . . .”FDA warning letter to Lovega LLC dba Pink Pony Peptides, Mar 31, 2026 · read the full letter on fda.gov ↗

What this is and is not.A warning letter is FDA’s statement of what it considers significant violations. It is an allegation, not a court finding, and the firm can respond. A closeout letter is posted when FDA confirms the violations were corrected.

Other GLP-1 letters FDA issued that week

Source

Every field above is copied from FDA’s page for this letter, read Oct 3, 2026. The letter on fda.gov ↗ · All 161 GLP-1 warning letters