Business · 09/09/2022Updated: 10/17/2026 · 1 min read
FDA Releases Draft Guidance on Labeling for Human Nonprescription Drug Products
The US Food and Drug Administration (FDA) has published a draft guidance document outlining recommended content and format for labeling human nonprescription drug products, aiming to enhance consumer comparison and self-selection.
Original source language: Federal Register — Food and Drug AdministrationOpen original release →