Home NDC 11822-0519-5 pain relief acetaminophen
Product NDC 11822-0519
Requested package NDC 11822-0519-5
11-digit product format 118220519
Labeler code 11822
Product ID 11822-0519_940fbb99-f563-43fe-bb35-0ca869fb8a6b
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen
Dosage form TABLET, COATED
Route ORAL
Labeler Rite Aid Corporation
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 acetaminophen
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 Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 11822-0519-1 pain relief acetaminophenExtra Strength 2 in 1 BLISTER PACK TABLET, COATED 2 24 11822-0519-1 pain relief acetaminophenExtra Strength 1 in 1 CARTON TABLET, COATED 1 24 11822-0519-2 pain relief acetaminophenExtra Strength 1 in 1 CARTON TABLET, COATED 1 24 11822-0519-2 pain relief acetaminophenExtra Strength 100 in 1 BOTTLE, PLASTIC TABLET, COATED 100 24 11822-0519-3 pain relief acetaminophenExtra Strength 225 in 1 BOTTLE, PLASTIC TABLET, COATED 225 24 11822-0519-5 pain relief acetaminophenExtra Strength 50 in 1 BOTTLE, PLASTIC TABLET, COATED 50 24 11822-0519-5 pain relief acetaminophenExtra Strength 1 in 1 CARTON TABLET, COATED 1 24 11822-0519-8 pain relief acetaminophenExtra Strength 1 in 1 CARTON TABLET, COATED 1 24 11822-0519-8 pain relief acetaminophenExtra Strength 24 in 1 BOTTLE, PLASTIC TABLET, COATED 24 24 11822-0519-9 pain relief acetaminophenExtra Strength 150 in 1 BOTTLE, PLASTIC TABLET, COATED 150 24
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 11822-0519 PAIN RELIEF ACETAMINOPHEN EXTRA STRENGTH (ACETAMINOPHEN) TABLET, COATED [RITE AID CORPORATION] 23 Current NDC, Legacy NDC, 10 package rows 20240928_26c0641e-1cdd-4084-939d-01dbd36ab9b7.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 77 · 1,530 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 11822-0519-5 11822051905 1 BOTTLE, PLASTIC in 1 CARTON (11822-0519-5) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC 2004-05-10 0000-00-00 No No Current