Home NDC 68998-070 Pain Relief
Product NDC 68998-070
11-digit product format 689980070
Labeler code 68998
Product ID 68998-070_25273d7c-8684-90d9-e063-6294a90aaeed
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen
Dosage form TABLET, COATED
Route ORAL
Labeler MARC GLASSMAN, INC.
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-09-15
Substance ACETAMINOPHEN
Active strength 500 mg/1
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 Pain Relief
Brand name suffix Extra Strength
Listing expiration 2026-12-31 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 RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 198440 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 68998-070-03 Pain ReliefExtra Strength 1 in 1 CARTON TABLET, COATED 1 3 68998-070-03 Pain ReliefExtra Strength 100 in 1 BOTTLE, PLASTIC TABLET, COATED 100 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 68998-070 PAIN RELIEF EXTRA STRENGTH (ACETAMINOPHEN) TABLET, COATED [MARC GLASSMAN, INC.] 3 Current NDC, Legacy NDC, 2 package rows 20241025_e23703bb-6087-7985-e053-2995a90aa5ec.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 Marketing start Marketing end Sample Exclude flag Status 68998-070-03 68998007003 1 BOTTLE, PLASTIC in 1 CARTON (68998-070-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC 2022-09-15 0000-00-00 No No Current