Home NDC 11822-0812-2 Pain Relief
Product NDC 11822-0812
Requested package NDC 11822-0812-2
11-digit product format 118220812
Labeler code 11822
Product ID 11822-0812_c301fedd-e98d-481b-8749-4156bb8383e5
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen
Dosage form TABLET, FILM COATED
Route ORAL
Labeler Rite Aid Corporation
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 1993-04-02
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 11822-0812-1 Pain ReliefExtra Strength 100 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 100 25 11822-0812-1 Pain ReliefExtra Strength 1 in 1 CARTON TABLET, FILM COATED 1 25 11822-0812-2 Pain ReliefExtra Strength 1 in 1 CARTON TABLET, FILM COATED 1 25 11822-0812-2 Pain ReliefExtra Strength 12 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 12 25 11822-0812-3 Pain ReliefExtra Strength 1 in 1 CARTON TABLET, FILM COATED 1 25 11822-0812-3 Pain ReliefExtra Strength 2 in 1 BLISTER PACK TABLET, FILM COATED 2 25 11822-0812-4 Pain ReliefExtra Strength 500 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 500 25 11822-0812-5 Pain ReliefExtra Strength 50 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 50 25 11822-0812-5 Pain ReliefExtra Strength 1 in 1 CARTON TABLET, FILM COATED 1 25 11822-0812-6 Pain ReliefExtra Strength 1 in 1 CARTON TABLET, FILM COATED 1 25 11822-0812-6 Pain ReliefExtra Strength 16 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 16 25 11822-0812-8 Pain ReliefExtra Strength 24 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 24 25 11822-0812-8 Pain ReliefExtra Strength 1 in 1 CARTON TABLET, FILM COATED 1 25
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 11822-0812 PAIN RELIEF EXTRA STRENGTH (ACETAMINOPHEN) TABLET, FILM COATED [RITE AID CORPORATION] 24 Current NDC, Legacy NDC, 13 package rows 20240911_d846065a-5c39-4f4b-894c-4280acaaf4fa.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 11822-0812-2 11822081202 1 BOTTLE, PLASTIC in 1 CARTON (11822-0812-2) / 12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC 1993-04-02 0000-00-00 No No Current