United States · FDA National Drug Code directory
Pain Relief 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
- 55910-834_0d05f2d6-747e-27e1-e063-6394a90a1797
- Product NDC
- 55910-834
- Form
- TABLET
- Composition / generic term
- Acetaminophen, Diphenhydramine HCl
- Labeler
- DOLGENCORP, INC.
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20231225
- 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 in 1 CARTON (55910-834-01) / 100 TABLET in 1 BOTTLE · 55910-834-01
- 1 BOTTLE in 1 CARTON (55910-834-05) / 50 TABLET in 1 BOTTLE · 55910-834-05
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 →