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
- 72476-171_1adb0e1c-a806-ed20-e063-6294a90a46ee
- Product NDC
- 72476-171
- Form
- TABLET, COATED
- Composition / generic term
- Acetaminophen and Diphenhydramine Hydrochloride
- Labeler
- RETAIL BUSINESS SERVICES , LLC.
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20240301
- 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
- 1 BOTTLE, PLASTIC in 1 CARTON (72476-171-01) / 20 TABLET, COATED in 1 BOTTLE, PLASTIC · 72476-171-01
- 1 BOTTLE, PLASTIC in 1 CARTON (72476-171-03) / 80 TABLET, COATED in 1 BOTTLE, PLASTIC · 72476-171-03
Source and coverage
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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.
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