Home NDC 55910-812-32 Pain Relief
Product NDC 55910-812
Requested package NDC 55910-812-32
11-digit product format 559100812
Labeler code 55910
Product ID 55910-812_9abdf7c4-281d-4d9d-86fb-541be4ea17bb
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen
Dosage form TABLET, COATED
Route ORAL
Labeler DOLGENCORP, LLC
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2004-05-10
Substance ACETAMINOPHEN
Active strength 500 mg/1
NDC exclude flag No
Listing certified through 2027-12-31
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 2027-12-31 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 55910-812-08 Pain ReliefExtra Strength 1 in 1 CARTON TABLET, COATED 1 20 55910-812-08 Pain ReliefExtra Strength 24 in 1 BOTTLE, PLASTIC TABLET, COATED 24 20 55910-812-32 Pain ReliefExtra Strength 120 in 1 BOTTLE, PLASTIC TABLET, COATED 120 20
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded ACETAMINOPHEN ACTIVE INGREDIENT 362O9ITL9D EXTRA STRENGTH PAIN RELIEF (ACETAMINOPHEN) CAPSULE, LIQUID FILLED [DOLGENCORP, LLC] 7 ACETAMINOPHEN ACTIVE MOIETY 362O9ITL9D EXTRA STRENGTH PAIN RELIEF (ACETAMINOPHEN) CAPSULE, LIQUID FILLED [DOLGENCORP, LLC] 7 CROSCARMELLOSE SODIUM INACTIVE INGREDIENT M28OL1HH48 EXTRA STRENGTH PAIN RELIEF (ACETAMINOPHEN) CAPSULE, LIQUID FILLED [DOLGENCORP, LLC] 7 D&C RED NO. 33 INACTIVE INGREDIENT 9DBA0SBB0L EXTRA STRENGTH PAIN RELIEF (ACETAMINOPHEN) CAPSULE, LIQUID FILLED [DOLGENCORP, LLC] 7 FD&C BLUE NO. 1 INACTIVE INGREDIENT H3R47K3TBD EXTRA STRENGTH PAIN RELIEF (ACETAMINOPHEN) CAPSULE, LIQUID FILLED [DOLGENCORP, LLC] 7 FD&C RED NO. 40 INACTIVE INGREDIENT WZB9127XOA EXTRA STRENGTH PAIN RELIEF (ACETAMINOPHEN) CAPSULE, LIQUID FILLED [DOLGENCORP, LLC] 7 FERRIC OXIDE YELLOW INACTIVE INGREDIENT EX438O2MRT EXTRA STRENGTH PAIN RELIEF (ACETAMINOPHEN) CAPSULE, LIQUID FILLED [DOLGENCORP, LLC] 7 FERROSOFERRIC OXIDE INACTIVE INGREDIENT XM0M87F357 EXTRA STRENGTH PAIN RELIEF (ACETAMINOPHEN) CAPSULE, LIQUID FILLED [DOLGENCORP, LLC] 7 GELATIN INACTIVE INGREDIENT 2G86QN327L EXTRA STRENGTH PAIN RELIEF (ACETAMINOPHEN) CAPSULE, LIQUID FILLED [DOLGENCORP, LLC] 7 HYDROXYPROPYL CELLULOSE INACTIVE INGREDIENT RFW2ET671P EXTRA STRENGTH PAIN RELIEF (ACETAMINOPHEN) CAPSULE, LIQUID FILLED [DOLGENCORP, LLC] 7 HYPROMELLOSES INACTIVE INGREDIENT 3NXW29V3WO EXTRA STRENGTH PAIN RELIEF (ACETAMINOPHEN) CAPSULE, LIQUID FILLED [DOLGENCORP, LLC] 7 POLYETHYLENE GLYCOLS INACTIVE INGREDIENT 3WJQ0SDW1A EXTRA STRENGTH PAIN RELIEF (ACETAMINOPHEN) CAPSULE, LIQUID FILLED [DOLGENCORP, LLC] 7 POVIDONE INACTIVE INGREDIENT FZ989GH94E EXTRA STRENGTH PAIN RELIEF (ACETAMINOPHEN) CAPSULE, LIQUID FILLED [DOLGENCORP, LLC] 7 PROPYLENE GLYCOL INACTIVE INGREDIENT 6DC9Q167V3 EXTRA STRENGTH PAIN RELIEF (ACETAMINOPHEN) CAPSULE, LIQUID FILLED [DOLGENCORP, LLC] 7 STEARIC ACID INACTIVE INGREDIENT 4ELV7Z65AP EXTRA STRENGTH PAIN RELIEF (ACETAMINOPHEN) CAPSULE, LIQUID FILLED [DOLGENCORP, LLC] 7 TITANIUM DIOXIDE INACTIVE INGREDIENT 15FIX9V2JP EXTRA STRENGTH PAIN RELIEF (ACETAMINOPHEN) CAPSULE, LIQUID FILLED [DOLGENCORP, LLC] 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 55910-812 PAIN RELIEF EXTRA STRENGTH (ACETAMINOPHEN) TABLET, COATED [DOLGENCORP, LLC] 19 Current NDC, Legacy NDC, 3 package rows 20240608_ce9f4e0d-43fb-499a-b8a2-a997a14841c4.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 55910-812-32 55910081232 120 TABLET, COATED in 1 BOTTLE, PLASTIC (55910-812-32) 2004-05-10 0000-00-00 No No Current