Is LL-37 FDA-approved?

No. LL-37 (ropocamptide) isn't FDA-approved, and Drugs@FDA lists no application with it as an active ingredient.

Checked 25 Oct 2026. The sources are below.

LL-37

Also: cathelicidin LL-37, CAMP peptide, ropocamptide

Status label in the Peptimes Library
Not FDA-Approved
Routes in Peptimes
SubcutaneousTopical
Updated
25 Oct 2026

US regulatory status

  • FDA status

    Not FDA-Approved. Drugs@FDA lists no application with LL-37 (ropocamptide) as an active ingredient.

    Source: Drugs@FDA, checked 25 Oct 2026

How to track it in Peptimes

Add LL-37 in My Protocols and set the schedule you already follow: days of the week, times of day and a start date. Peptimes never suggests an amount when you log or schedule a dose. Its Library entry shows the status label “Not FDA-Approved”.

  • Routes: subcutaneous or topical. Choose the one that matches each dose.
  • Logging: the amount you took, the route and how you feel.
  • Injection sites: subcutaneous doses record the site, and Insights shows where you’ve injected and how recently. It never suggests where to inject next. Topical doses skip this step.
  • Reminders and history: reminders at your times, Dose History, the Calendar and CSV or JSON export work as described on the peptide tracker app page.

Peptimes is a tracking app, not medical advice. Talk to a licensed clinician about your treatment. Peptimes doesn’t sell LL-37 or any other compound.

More sources

  • FDA, Global Substance Registration System, Ropocamptide, checked 25 Oct 2026: its sequence of 37 amino acids, and the names LL-37, cathelicidin LL-37 and ropocamptide.

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