Business · 13/01/2005
FDA Releases Draft Guidance for Labeling Over-the-Counter Human Drug Products
The Food and Drug Administration (FDA) has published a draft guidance to help manufacturers, packers, and distributors of over-the-counter (OTC) human drug products comply with new labeling regulations, which include standardized content and format requirements.
Original source language: Federal Register — Food and Drug AdministrationOpen original release →