United States · FDA National Drug Code directory
acetaminophen pm extra strength
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
- 41163-515_24b11c3b-9c19-ff00-e063-6394a90adbed
- Product NDC
- 41163-515
- Form
- TABLET, COATED
- Composition / generic term
- Acetaminophen and Diphenhydramine Hydrochloride
- Labeler
- United Natural Foods, Inc. dba UNFI
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20140901
- 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 (41163-515-01) / 24 TABLET, COATED in 1 BOTTLE, PLASTIC · 41163-515-01
- 1 BOTTLE, PLASTIC in 1 CARTON (41163-515-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC · 41163-515-03
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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