Home NDC 11822-0812 Pain Relief
Product NDC 11822-0812
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 Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 2 · 61 matching rows.
View current auxiliary records. · View the auxiliary file history.
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 37 of 79 · 1,570 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Pain Relief PM Extra Strength ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE TopCo Associates LLC 3b672ec7-8658-4b43-a79d-094ac8bc6904 2025-09-29 Warnings Exact identifier application number: M013 kirkland signature acetaminophen adult extra strength ACETAMINOPHEN Costco Wholesale Company a9979167-1a82-47d7-9602-2865f9bdd628 2025-09-27 Warnings Exact identifier application number: M013 First Aid Direct Chewable Aspirin ASPIRIN Cintas Corp ff6960f6-9f55-4f32-9ab5-9187724531e9 2025-09-25 Warnings Exact identifier application number: M013 Bayer Rapid Relief Body Pain ASPIRIN/CAFFEINE ORAL POWDER Bayer HealthCare LLC. 3fa1ec07-d1a6-226b-e063-6394a90a3213 2025-09-25 Warnings Exact identifier application number: M013 Xpect Chewable Aspirin ASPIRIN Cintas Corporation bddce374-1d35-4685-987d-4a4cc9994155 2025-09-25 Warnings Exact identifier application number: M013 IBUPROFEN IBUPROFEN Kroger Company bbedfc37-913d-8046-e053-2995a90af68a 2025-09-24 Warnings Exact identifier application number: M013 Xpect Pain Away Extra Strength ACETAMINOPHEN ASPIRIN CAFFEINE Cintas Corporation 1269d069-afaf-4ca5-b369-f74249a348db 2025-09-24 Warnings Exact identifier application number: M013 Aspirin Low Dose ASPIRIN Preferred Pharmaceuticals Inc. 29214eec-860c-43f0-83c6-9ed5a9f530af 2025-09-22 Warnings Exact identifier application number: M013 ASPIRIN ASPIRIN Kroger Company bbee8ee4-e09d-3ba6-e053-2a95a90af647 2025-09-19 Warnings Exact identifier application number: M013 careone acetaminophen ACETAMINOPHEN American Sales Company 4bb696f6-a47b-4da9-9224-9aeae3e152f3 2025-09-19 Warnings Exact identifier application number: M013 Childrens Pain Relief ACETAMINOPHEN Aurohealth LLC 49a740ec-8ed4-4c76-b2d0-c13651bafa5e 2025-09-18 Warnings Exact identifier application number: M013 Extra Strength Headache Relief ACETAMINOPHEN, ASPIRIN, AND CAFFEINE Advanced Rx LLC a7ed4c76-a5b5-44f7-866f-f43790e45c78 2025-09-18 Warnings Exact identifier application number: M013 acetaminophen ACETAMINOPHEN CVS Pharmacy fc2d4367-8884-4b76-aa3e-8c35be1ace49 2025-09-18 Warnings Exact identifier application number: M013 Aspirin Enteric Coated, Regular Strength ASPIRIN Walgreen Company 5e1484d3-5be1-40da-a3bf-fb19f7d27d45 2025-09-18 Warnings Exact identifier application number: M013 TYLENOL Extra Strength ACETAMINOPHEN Kenvue Brands LLC ab02080a-c903-4e4a-a9f3-2b8197ed2f2b 2025-09-17 Warnings Exact identifier application number: M013 Childrens TYLENOL ACETAMINOPHEN Kenvue Brands LLC 79669930-f744-4bb1-8325-b75951489b64 2025-09-17 Warnings Exact identifier application number: M013 Pain Reliever PM Extra Strength ACETAMINOPHEN, DIPHENHYDRAMINE HCL L.N.K. International, Inc. ff199db8-c7ea-4b6e-ad8b-3ceeca883d92 2025-09-15 Warnings Exact identifier application number: M013 Acetaminophen PM Extra Strength ACETAMINOPHEN, DIPHENHYDRAMINE HCL FOODHOLD U.S.A., LLC fdd7ce80-d6be-41b9-affd-d024cf306b50 2025-09-12 Warnings Exact identifier application number: M013 Extra Strength Pain Reliever ACETAMINOPHEN INGLES MARKETS, INC. 3e89240b-0e27-fde4-e063-6394a90a779f 2025-09-11 Warnings Exact identifier application number: M013 Aspirin 81 mg Low Dose ASPIRIN HEB 926fe7b6-9607-469f-912f-4019891067a9 2025-09-10 Warnings Exact identifier application number: M013
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 11822-0812-1 11822081201 1 BOTTLE, PLASTIC in 1 CARTON (11822-0812-1) > 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC 1993-04-02 0000-00-00 No No Current 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 11822-0812-3 11822081203 1 BLISTER PACK in 1 CARTON (11822-0812-3) > 2 TABLET, FILM COATED in 1 BLISTER PACK 1 blister pack 1993-04-02 0000-00-00 No No Current 11822-0812-4 11822081204 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (11822-0812-4) 1993-04-02 0000-00-00 No No Current 11822-0812-5 11822081205 1 BOTTLE, PLASTIC in 1 CARTON (11822-0812-5) > 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC 1993-04-02 0000-00-00 No No Current 11822-0812-6 11822081206 1 BOTTLE, PLASTIC in 1 CARTON (11822-0812-6) > 16 TABLET, FILM COATED in 1 BOTTLE, PLASTIC 1993-04-02 2021-10-08 No No Current 11822-0812-8 11822081208 1 BOTTLE, PLASTIC in 1 CARTON (11822-0812-8) > 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC 1993-04-02 0000-00-00 No No Current