Home NDC 79903-099 Nighttime Pain Reliever plus Sleep Aid
Product NDC 79903-099
11-digit product format 799030099
Labeler code 79903
Product ID 79903-099_80974088-72ac-4a5b-aabf-33e0424f9696
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen, Diphenhydramine HCl
Dosage form SOLUTION
Route ORAL
Labeler WALMART INC.
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-01-12
Substance ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE
Active strength 1000; 50 mg/30mL; mg/30mL
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 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 Nighttime Pain Reliever plus Sleep Aid
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACETAMINOPHEN 1000 mg/30mL DIPHENHYDRAMINE HYDROCHLORIDE 50 mg/30mL
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 1092373 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 79903-099-02 Nighttime Pain Reliever plus Sleep Aid 355 mL in 1 BOTTLE, PLASTIC SOLUTION 355 9
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 79903-099 NIGHTTIME PAIN RELIEVER PLUS SLEEP AID (ACETAMINOPHEN, DIPHENHYDRAMINE HCL) SOLUTION [WALMART INC.] 8 Current NDC, Legacy NDC, 1 package rows 20250302_8dd85a6b-507c-4502-9e55-a40bdf21d379.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 21 of 79 · 1,579 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 79903-099-02 79903009902 355 mL in 1 BOTTLE, PLASTIC (79903-099-02) 355 ml 2022-01-12 0000-00-00 No No Current