Home NDC 59726-494 Pain Relief
Product NDC 59726-494
11-digit product format 597260494
Labeler code 59726
Product ID 59726-494_911f8255-5be5-4012-b398-f2c9e74dc4a8
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen
Dosage form TABLET
Route ORAL
Labeler P & L Development, LLC
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2016-03-31
Marketing end 2026-12-31
Substance ACETAMINOPHEN
Active strength 500 mg/1
NDC exclude flag No
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 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 59726-494-05 Pain ReliefExtra Strength 1 in 1 BOX TABLET 1 10 59726-494-05 Pain ReliefExtra Strength 500 in 1 BOTTLE, PLASTIC TABLET 500 10 59726-494-10 Pain ReliefExtra Strength 100 in 1 BOTTLE, PLASTIC TABLET 100 10 59726-494-24 Pain ReliefExtra Strength 24 in 1 BOTTLE, PLASTIC TABLET 24 10 59726-494-24 Pain ReliefExtra Strength 1 in 1 BOX TABLET 1 10 59726-494-50 Pain ReliefExtra Strength 50 in 1 BOTTLE, PLASTIC TABLET 50 10 59726-494-50 Pain ReliefExtra Strength 1 in 1 BOX TABLET 1 10
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 59726-494 PAIN RELIEF EXTRA STRENGTH (ACETAMINOPHEN) TABLET [P & L DEVELOPMENT, LLC] 9 Current NDC, Legacy NDC, 7 package rows 20240418_59eb14a5-40b0-4331-beb5-7166e6cdf411.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 39 of 79 · 1,576 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 59726-494-05 59726049405 1 BOTTLE, PLASTIC in 1 BOX (59726-494-05) / 500 TABLET in 1 BOTTLE, PLASTIC 2016-03-31 2026-12-31 No No Current 59726-494-10 59726049410 100 TABLET in 1 BOTTLE, PLASTIC (59726-494-10) 100 tablet 2016-03-31 2026-12-31 No No Current 59726-494-24 59726049424 1 BOTTLE, PLASTIC in 1 BOX (59726-494-24) / 24 TABLET in 1 BOTTLE, PLASTIC 2016-03-31 2026-12-31 No No Current 59726-494-50 59726049450 1 BOTTLE, PLASTIC in 1 BOX (59726-494-50) / 50 TABLET in 1 BOTTLE, PLASTIC 2016-03-31 2026-12-31 No No Current