Home NDC 66715-6867 Pain Reliever
Product NDC 66715-6867
11-digit product format 667156867
Labeler code 66715
Product ID 66715-6867_2a929624-4394-458a-e063-6394a90afbf2
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen 500 mg, film-coated tablet
Dosage form TABLET, FILM COATED
Route ORAL
Labeler Lil' Drug Store Products, Inc.
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-03-04
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 Reliever
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 66715-6867-4 Pain Reliever 1 in 1 CARTON TABLET, FILM COATED 1 3 66715-6867-4 Pain Reliever 24 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 24 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 66715-6867 PAIN RELIEVER (ACETAMINOPHEN 500 MG, FILM-COATED TABLET) TABLET, FILM COATED [LIL' DRUG STORE PRODUCTS, INC.] 3 Current NDC, Legacy NDC, 2 package rows 20250101_e5f9def4-4cf5-4e06-e053-2995a90a07ea.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 66715-6867-4 66715686704 1 BOTTLE, PLASTIC in 1 CARTON (66715-6867-4) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC 2022-03-04 0000-00-00 No No Current