Home NDC 36800-905 Pain Relief
Product NDC 36800-905
11-digit product format 368000905
Labeler code 36800
Product ID 36800-905_2850a74e-12a4-88d3-e063-6394a90a831b
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen
Dosage form TABLET
Route ORAL
Labeler TopCo Associates LLC
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2011-08-30
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 Relief
Brand name suffix Extra Strength
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 36800-905-02 Pain ReliefExtra Strength 1 in 1 CARTON TABLET 1 4 36800-905-02 Pain ReliefExtra Strength 60 in 1 BOTTLE, PLASTIC TABLET 60 4 36800-905-04 Pain ReliefExtra Strength 100 in 1 BOTTLE, PLASTIC TABLET 100 4 36800-905-04 Pain ReliefExtra Strength 1 in 1 CARTON TABLET 1 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 36800-905 PAIN RELIEF EXTRA STRENGTH (ACETAMINOPHEN) TABLET [TOPCO ASSOCIATES LLC] 4 Current NDC, Legacy NDC, 4 package rows 20241204_bdb01b3e-ad34-4003-9b9a-e83a2c0e90bb.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 Marketing start Marketing end Sample Exclude flag Status 36800-905-02 36800090502 1 BOTTLE, PLASTIC in 1 CARTON (36800-905-02) / 60 TABLET in 1 BOTTLE, PLASTIC 2011-08-30 0000-00-00 No No Current 36800-905-04 36800090504 1 BOTTLE, PLASTIC in 1 CARTON (36800-905-04) / 100 TABLET in 1 BOTTLE, PLASTIC 2011-08-30 0000-00-00 No No Current