Home NDC 79903-267 Acetaminophen and Diphenhydramine hydrochloride
Product NDC 79903-267
11-digit product format 799030267
Labeler code 79903
Product ID 79903-267_d57e57bb-b700-4f99-9e22-1e887bd85515
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen and Diphenhydramine hydrochloride
Dosage form TABLET
Route ORAL
Labeler WALMART INC.
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-06-28
Substance ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE
Active strength 500; 25 mg/1; mg/1
Pharmacologic classes Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Acetaminophen and Diphenhydramine hydrochloride
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACETAMINOPHEN 500 mg/1 DIPHENHYDRAMINE HYDROCHLORIDE 25 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 362O9ITL9D Internal UNII lookup TC2D6JAD40 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1092189 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 79903-267-80 Acetaminophen and Diphenhydramine hydrochloride 80 in 1 BOTTLE TABLET 80 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 79903-267 ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE TABLET [WALMART INC.] 2 Current NDC, 1 package rows 20240704_16d5786c-2346-f970-e063-6394a90a0a8c.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 83 · 1,657 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 79903-267-80 79903026780 80 TABLET in 1 BOTTLE (79903-267-80) 80 tablet 2024-06-28 No No Current