Home NDC 30142-507 Acetaminophen
Product NDC 30142-507
11-digit product format 301420507
Labeler code 30142
Product ID 30142-507_4244c2ed-f273-4caa-a411-3f40e32a2f25
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen
Dosage form TABLET, FILM COATED
Route ORAL
Labeler Kroger Company
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2015-08-18
Substance ACETAMINOPHEN
Active strength 500 mg/1
NDC exclude flag No
Listing certified through 2026-12-31
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 · 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 Acetaminophen
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 30142-507-62 Acetaminophen 24 in 1 BOTTLE TABLET, FILM COATED 24 6 30142-507-62 Acetaminophen 1 in 1 CARTON TABLET, FILM COATED 1 6 30142-507-78 Acetaminophen 1 in 1 CARTON TABLET, FILM COATED 1 6 30142-507-78 Acetaminophen 100 in 1 BOTTLE TABLET, FILM COATED 100 6 30142-507-83 Acetaminophen 1 in 1 CARTON TABLET, FILM COATED 1 6 30142-507-83 Acetaminophen 225 in 1 BOTTLE TABLET, FILM COATED 225 6
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded ACETAMINOPHEN ACTIVE INGREDIENT 362O9ITL9D ACETAMINOPHEN CAPSULE, COATED [KROGER COMPANY] 1 ACETAMINOPHEN ACTIVE MOIETY 362O9ITL9D ACETAMINOPHEN CAPSULE, COATED [KROGER COMPANY] 1 CROSCARMELLOSE SODIUM INACTIVE INGREDIENT M28OL1HH48 ACETAMINOPHEN CAPSULE, COATED [KROGER COMPANY] 1 CROSPOVIDONE INACTIVE INGREDIENT 68401960MK ACETAMINOPHEN CAPSULE, COATED [KROGER COMPANY] 1 HYPROMELLOSES INACTIVE INGREDIENT 3NXW29V3WO ACETAMINOPHEN CAPSULE, COATED [KROGER COMPANY] 1 POLYETHYLENE GLYCOLS INACTIVE INGREDIENT 3WJQ0SDW1A ACETAMINOPHEN CAPSULE, COATED [KROGER COMPANY] 1 POLYSORBATE 80 INACTIVE INGREDIENT 6OZP39ZG8H ACETAMINOPHEN CAPSULE, COATED [KROGER COMPANY] 1 POVIDONES INACTIVE INGREDIENT FZ989GH94E ACETAMINOPHEN CAPSULE, COATED [KROGER COMPANY] 1 STEARIC ACID INACTIVE INGREDIENT 4ELV7Z65AP ACETAMINOPHEN CAPSULE, COATED [KROGER COMPANY] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 30142-507 ACETAMINOPHEN TABLET, FILM COATED [KROGER COMPANY] 6 Current NDC, Legacy NDC, 6 package rows 20241027_5bfd9841-c781-43be-b823-d334893ae6ed.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 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 30142-507-62 30142050762 1 BOTTLE in 1 CARTON (30142-507-62) > 24 TABLET, FILM COATED in 1 BOTTLE 1 bottle 2015-08-18 2023-02-28 No No Current 30142-507-78 30142050778 1 BOTTLE in 1 CARTON (30142-507-78) / 100 TABLET, FILM COATED in 1 BOTTLE 1 bottle 2015-08-18 0000-00-00 No No Current 30142-507-83 30142050783 1 BOTTLE in 1 CARTON (30142-507-83) / 225 TABLET, FILM COATED in 1 BOTTLE 1 bottle 2015-08-21 0000-00-00 No No Current