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
- 41163-956_341c4641-167b-42ef-998a-9e2a0df7404b
- Product NDC
- 41163-956
- Form
- TABLET, COATED
- Composition / generic term
- Acetaminophen, Diphenhydramine HCl
- Labeler
- United Natural Foods, Inc. dba UNFI
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20071217
- 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
- 1 BOTTLE, PLASTIC in 1 CARTON (41163-956-09) / 20 TABLET, COATED in 1 BOTTLE, PLASTIC · 41163-956-09
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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