Business · 05/01/2009Updated: 10/17/2026 · 1 min read
FDA Releases Guidance for Industry on Labeling OTC Human Drug Products
Summary
The Food and Drug Administration (FDA) has published a guidance document to help manufacturers, packers, and distributors of over-the-counter (OTC) human drugs comply with the agency's labeling regulations, which became effective after a previously finalized draft guidance was updated.
Original source language: Federal Register — Food and Drug AdministrationOpen original release →