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Business · 09/12/2004Updated: 10/17/2026 · 1 min read

FDA Releases Draft Guidance for Small Businesses on Labeling OTC Human Drug Products

The Food and Drug Administration (FDA) has made available a draft compliance guide to assist small businesses in meeting the new labeling requirements for over-the-counter human drug products, with implementation deadlines set for later this year.

Original source language: Federal Register — Food and Drug AdministrationOpen original release →

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