Home NDC 83324-081-01 Pain Relief
Product NDC 83324-081
Requested package NDC 83324-081-01
11-digit product format 833240081
Labeler code 83324
Product ID 83324-081_1ac6e721-4d0a-0396-e063-6294a90a7fe9
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen
Dosage form TABLET
Route ORAL
Labeler Chain Drug Marketing Association
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-04-26
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 83324-081-01 Pain ReliefExtra Strength 100 in 1 PACKAGE TABLET 100 2 83324-081-01 Pain ReliefExtra Strength 1 in 1 CARTON TABLET 1 2 83324-081-10 Pain ReliefExtra Strength 100 in 1 BOTTLE, PLASTIC TABLET 100 2 83324-081-60 Pain ReliefExtra Strength 60 in 1 BOTTLE, PLASTIC TABLET 60 2 83324-081-60 Pain ReliefExtra Strength 1 in 1 CARTON TABLET 1 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 83324-081 PAIN RELIEF EXTRA STRENGTH (ACETAMINOPHEN) TABLET [CHAIN DRUG MARKETING ASSOCIATION] 2 Current NDC, 5 package rows 20240615_cfaf9495-e654-4dfc-ba23-d2358c3720c4.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 Units Marketing start Sample Exclude flag Status 83324-081-01 83324008101 1 PACKAGE in 1 CARTON (83324-081-01) / 100 TABLET in 1 PACKAGE 1 package 2024-04-26 No No Current