United States · FDA National Drug Code directory
ACETAMINOPHEN 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
- 73057-352_2c27d537-a03c-3775-e063-6394a90ad003
- Product NDC
- 73057-352
- Form
- TABLET, FILM COATED
- Composition / generic term
- Acetaminophen 500mg / Diphenhydramine HCl 25mg
- Labeler
- Ulai Health LLC
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20190708
- Source listing expiry
- 20261231
Source-listed ingredients
- ACETAMINOPHEN — 500 mg/1
- DIPHENHYDRAMINE HYDROCHLORIDE — 25 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (73057-352-03) · 73057-352-03
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 →