Acetaminophen Diphenhydramine HCL

Dr. Reddy's Laboratories Inc.🇺🇸 United States

FDA Page

Effective Date: Sep 15, 2026
Approval ID: cec0e5c9-0470-4a5e-b552-77d0dc117bdd
Products: 0 registered
Version: 1

Regulatory Information

Labeling Type

HUMAN OTC DRUG LABEL

Status

Approved

Full Title

Extra StrengthAcetaminophen PM Acetaminophen USP, 500 mg / Pain reliever Diphenhydramine HCl USP, 25 mg / Nighttime sleep-aidNon-habit formingContains no aspirin

Quick Stats

Total Products0

Labelers1

Label Sections20

Regulatory Agency

🇺🇸

U.S. Food and Drug Administration

United States

Data Sources & Disclaimer: Approval information is sourced from official FDA databases. This content is for informational purposes only and does not constitute medical or regulatory advice. Always refer to official FDA websites for the most current information.