Home NDC 79903-307 Pain Reliever PM
Product NDC 79903-307
11-digit product format 799030307
Labeler code 79903
Product ID 79903-307_1b781b66-7c7a-489c-afd0-cb525474df6c
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen, Diphenhydramine HCl
Dosage form TABLET, FILM COATED
Route ORAL
Labeler WALMART INC.
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-01-23
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 2027-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Pain Reliever PM
Listing expiration 2027-12-31 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 79903-307-10 Pain Reliever PM 100 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 100 5 79903-307-11 Pain Reliever PM 100 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 100 5 79903-307-24 Pain Reliever PM 24 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 24 5 79903-307-24 Pain Reliever PM 1 in 1 CARTON TABLET, FILM COATED 1 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 79903-307 PAIN RELIEVER PM (ACETAMINOPHEN, DIPHENHYDRAMINE HCL) TABLET, FILM COATED [WALMART INC.] 2 Current NDC, 4 package rows 20250124_42310898-cf3a-4ffb-88bb-b8b84449156e.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 85 · 1,687 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 79903-307-10 79903030710 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-307-10) 2025-01-23 2029-03-31 No No Historical 79903-307-11 79903030711 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-307-11) 2026-04-08 No No Current 79903-307-24 79903030724 1 BOTTLE, PLASTIC in 1 CARTON (79903-307-24) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC 2025-11-25 No No Current