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Activities & Initiatives
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Chemical Restrictions in Children’s Products

Lawmakers should support the centralized progress made on ingredient evaluation, labeling, and packaging protections by specialized national children’s health agencies instead of allowing jurisdiction confusion that ultimately hinders healthcare advancement for all ages.

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Multimedia
Same Sex Couple with Their Baby in the kitchen

FAQs

FAQs About HSA/FSA Accounts and the CARES Act
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FDA Annual Forecast

The Annual Forecast for Planned Monograph Activities describes planned monograph activities that FDA intends to address over the ensuing three years.

Flask with Chemicals in Gloved Hand
Critical Ingredients & Chemicals

Federal oversight by the FDA ensures that ingredients and chemical additives used in vital healthcare products available to consumers, like nonprescription drugs, dietary supplements, and medical devices, routinely undergo the most rigorous safety evaluations.

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Safe Use of Acetaminophen

Safe use of acetaminophen is a top priority for manufacturers of OTC medicines. Manufacturers work closely with FDA, healthcare provider groups, pharmacist groups, and consumer health advocates to drive safe and responsible use of acetaminophen.

hands in sterile gloves holding manufactured white tablets

Industry Self-Regulation for Dietary Supplements

Dietary Supplement Component Supplier Qualification

This document serves as a voluntary guideline to assist manufacturers of dietary supplements with compliance with the dietary supplement current good manufacturing practice (cGMP) requirements of the US FDA 21 CFR §111.

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FAQs

FAQs About Homeopathic Medicine

Learn about the uses, safety, and regulation of homeopathic medicines in the U.S.

Medicine bottle, syringe, and dosing cup with purple liquid medicine
Background Summary: Risks Associated with Codeine-Containing Cough Medicine

This Proposed Safety Administrative Order addresses the GRASE status of codeine, codeine phosphate, and codeine sulfate as antitussive active ingredients.

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