What FDA’s record states
| Field | What FDA’s record states | Source |
|---|---|---|
| Recipient | Lovega LLC dba Pink Pony Peptides | FDA letter ↗ |
| Location | Wellington, FL | FDA letter ↗ |
| Letter date | Mar 31, 2026 | FDA letter ↗ |
| Posted by FDA | Apr 7, 2026 | FDA index ↗ |
| Issuing office | Center for Drug Evaluation and Research (CDER) | FDA letter ↗ |
| Subject | Unapproved New Drugs Sold Over the Internet | FDA letter ↗ |
| MARCS-CMS number | 721088 | FDA letter ↗ |
| GLP-1 drugs named | Tirzepatide, Retatrutide | FDA letter ↗ |
| Response letter | Not published by FDA | FDA letter ↗ |
| Closeout letter | Not published by FDA | FDA 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