United States · FDA National Drug Code directory
Pain Reliever PM
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 79903-307_1f12d953-6e7f-46c1-bcb8-59dae3bec38f
- Product NDC
- 79903-307
- Form
- TABLET, FILM COATED
- Composition / generic term
- Acetaminophen, Diphenhydramine HCl
- Labeler
- WALMART INC.
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20250123
- Source listing expiry
- 20271231
Source-listed ingredients
- ACETAMINOPHEN — 500 mg/1
- DIPHENHYDRAMINE HYDROCHLORIDE — 25 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-307-10) · 79903-307-10
- 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-307-11) · 79903-307-11
- 1 BOTTLE, PLASTIC in 1 CARTON (79903-307-24) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC · 79903-307-24
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →