Home NDC 79903-422 equate pain relief
Product NDC 79903-422
11-digit product format 799030422
Labeler code 79903
Product ID 79903-422_92d99ee1-dff8-4f7b-a7cf-9f7fe65ee175
Type HUMAN OTC DRUG
Nonproprietary name acetaminophen
Dosage form LIQUID
Route ORAL
Labeler WALMART INC.
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-04-29
Substance ACETAMINOPHEN
Active strength 1000 mg/30mL
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 equate pain relief
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACETAMINOPHEN 1000 mg/30mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 362O9ITL9D Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 307684 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 79903-422-12 79903042212 355 mL in 1 BOTTLE (79903-422-12) 355 ml 2026-04-29 No No Current