Home NDC 69842-931 Acetaminophen
Product NDC 69842-931
11-digit product format 698420931
Labeler code 69842
Product ID 69842-931_4f2412fc-ac45-48f3-bc00-9c1f9e30cec6
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen
Dosage form TABLET, FILM COATED
Route ORAL
Labeler CVS PHARMACY
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2005-12-11
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 Acetaminophen
Brand name suffix Extra Strength
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 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 69842-931-08 AcetaminophenExtra Strength 24 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 24 17 69842-931-08 AcetaminophenExtra Strength 1 in 1 CARTON TABLET, FILM COATED 1 17 69842-931-17 AcetaminophenExtra Strength 300 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 300 17 69842-931-29 AcetaminophenExtra Strength 150 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 150 17
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69842-931 ACETAMINOPHEN EXTRA STRENGTH (ACETAMINOPHEN) TABLET, FILM COATED [CVS PHARMACY] 16 Current NDC, Legacy NDC, 4 package rows 20250519_64a1ebe7-af28-4b09-96e8-28fa4dcc52bd.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 63 of 79 · 1,579 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 69842-931-08 69842093108 1 BOTTLE, PLASTIC in 1 CARTON (69842-931-08) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC 2005-12-11 0000-00-00 No No Current 69842-931-17 69842093117 300 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69842-931-17) 2005-12-11 0000-00-00 No No Current 69842-931-29 69842093129 150 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69842-931-29) 2005-12-11 2027-01-31 No No Current