Home NDC 69842-449 Pain Relief
Product NDC 69842-449
11-digit product format 698420449
Labeler code 69842
Product ID 69842-449_14c313b7-0026-4f9b-a730-79d73145ed10
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen
Dosage form TABLET, CHEWABLE
Route ORAL
Labeler CVS PHARMACY
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2005-01-28
Marketing end 2027-10-31
Substance ACETAMINOPHEN
Active strength 160 mg/1
NDC exclude flag No
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 · 12 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…
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 childrens Active Ingredients# Ingredient, Strength table Ingredient Strength ACETAMINOPHEN 160 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 313820 Internal RxNorm 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 69842-449-08 Pain Reliefchildrens 4 in 1 CARTON TABLET, CHEWABLE 4 14 69842-449-08 Pain Reliefchildrens 6 in 1 BLISTER PACK TABLET, CHEWABLE 6 14 69842-449-95 Pain Reliefchildrens 24 in 1 BOTTLE, PLASTIC TABLET, CHEWABLE 24 14 69842-449-95 Pain Reliefchildrens 1 in 1 CARTON TABLET, CHEWABLE 1 14
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69842-449 PAIN RELIEF CHILDRENS (ACETAMINOPHEN) TABLET, CHEWABLE [CVS PHARMACY] 13 Current NDC, Legacy NDC, 4 package rows 20250217_b8ab85a6-3eab-4ef4-a13d-5ac300480f63.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 60 of 79 · 1,579 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 69842-449-08 69842044908 4 BLISTER PACK in 1 CARTON (69842-449-08) > 6 TABLET, CHEWABLE in 1 BLISTER PACK 4 blister pack 2005-01-28 2022-07-29 No No Current 69842-449-95 69842044995 1 BOTTLE, PLASTIC in 1 CARTON (69842-449-95) / 24 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC 2005-01-28 2027-10-31 No No Current