MONITORFEDGLP-1 CompoundingFeb 23, 2026

FDA / Federal Register Notice: Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Human Drug Compounding Under Sections 503A and 503B of the Federal Food, Drug, and Cosmetic Act

New FDA notice may impact GLP-1 compounding practices at med spas.

What changed & why it matters

Med Spa Radar recorded a Federal Register notice at the federal level, dated February 23, 2026, in the GLP-1 Compounding category.

Federal Register activity is where federal compounding policy is actually written — proposed rules, comment periods, and clinical-need determinations that decide which bulk substances may be compounded under sections 503A and 503B.

Type
Federal Register
Jurisdiction
Federal
Category
GLP-1 Compounding
Recorded
February 23, 2026

What this means for your specific practice — the exact step to take, the deadline to calendar, or the supplier detail to check — is in the member "what to do" below. This page is the free record of what changed and why it matters.

What to do

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Federal Register · primary source ↗

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Monitoring, not legal advice.