Business · 24/02/2009Updated: 10/17/2026 · 1 min read
FDA Requests Comments on Labeling of Nonprescription Human Drug Products
Summary
The Food and Drug Administration (FDA) is seeking public comment on proposed information collection activities related to labeling requirements for nonprescription human drug products, as mandated by the Dietary Supplement and Nonprescription Drug Consumer Protection Act of 1995.
Original source language: Federal Register — Food and Drug AdministrationOpen original release →