Business · 09/04/1998Updated: 10/17/2026 · 1 min read
FDA Releases Guidance on Ingredient Listing for Over-the-Counter (OTC) Drugs
Summary
The Food and Drug Administration (FDA) has made available a guidance document outlining the administrative processes for implementing the Food and Drug Administration Modernization Act of 1997 (FDAMA) regarding ingredient listing for OTC drugs.
Original source language: Federal Register — Food and Drug AdministrationOpen original release →