Home NDC 53942-170-03 Pain Relief
Product NDC 53942-170
Requested package NDC 53942-170-03
11-digit product format 539420170
Labeler code 53942
Product ID 53942-170_5fdce7e2-4438-b097-e063-6394a90a836f
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen
Dosage form TABLET, COATED
Route ORAL
Labeler Demoulas Super Markets, Inc
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-07-16
Substance ACETAMINOPHEN
Active strength 500 mg/1
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 Pain Relief
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACETAMINOPHEN 500 mg/1
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 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 53942-170-13 Pain Relief 225 in 1 BOTTLE, PLASTIC TABLET, COATED 225 2
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 77 · 1,530 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Sample Exclude flag Status 53942-170-03 53942017003 1 BOTTLE, PLASTIC in 1 CARTON (53942-170-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC 2026-11-09 No No Current