Home NDC 69842-750-96 Acetaminophen
Product NDC 69842-750
Requested package NDC 69842-750-96
11-digit product format 698420750
Labeler code 69842
Product ID 69842-750_f96cefa0-5a08-4358-b900-2428afef4ffb
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 1993-04-02
Substance ACETAMINOPHEN
Active strength 500 mg/1
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 1 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 69842-750 69842-750-96 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…
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 69842-750-03 AcetaminophenExtra Strength 1 in 1 PACKAGE TABLET, FILM COATED 1 13 69842-750-03 AcetaminophenExtra Strength 10 in 1 BOTTLE TABLET, FILM COATED 10 13 69842-750-96 AcetaminophenExtra Strength 2 in 1 PACKAGE TABLET, FILM COATED 2 13 69842-750-96 AcetaminophenExtra Strength 10 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 10 13
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69842-750 ACETAMINOPHEN EXTRA STRENGTH (ACETAMINOPHEN) TABLET, FILM COATED [CVS PHARMACY] 11 Current NDC, Legacy NDC, 4 package rows 20250428_afacdc0b-fb65-464e-91b8-e82ba7ecde44.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 69842-750-96 69842075096 2 BOTTLE, PLASTIC in 1 PACKAGE (69842-750-96) > 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC 1993-04-02 0000-00-00 No No Current