Home NDC 11822-0600 Pain Relief Aspirin
Product NDC 11822-0600
11-digit product format 118220600
Labeler code 11822
Product ID 11822-0600_03139c1b-6cee-4d3c-89dd-b07596d75ee7
Type HUMAN OTC DRUG
Nonproprietary name Aspirin
Dosage form TABLET, DELAYED RELEASE
Route ORAL
Labeler Rite Aid Corporation
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2008-02-12
Substance ASPIRIN
Active strength 81 mg/1
Pharmacologic classes Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Decreased Platelet Aggregation [PE], Decreased Prostaglandin Production [PE], Nonsteroidal Anti-inflammatory Drug [EPC], Platelet Aggregation Inhibitor [EPC]
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 Aspirin
Brand name suffix Low Dose
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ASPIRIN 81 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination R16CO5Y76E Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 308416 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 11822-0600-2 Pain Relief AspirinLow Dose 1 in 1 CARTON TABLET, DELAYED RELEASE 1 19 11822-0600-2 Pain Relief AspirinLow Dose 32 in 1 BOTTLE, PLASTIC TABLET, DELAYED RELEASE 32 19 11822-0600-3 Pain Relief AspirinLow Dose 120 in 1 BOTTLE, PLASTIC TABLET, DELAYED RELEASE 120 19 11822-0600-3 Pain Relief AspirinLow Dose 1 in 1 CARTON TABLET, DELAYED RELEASE 1 19 11822-0600-4 Pain Relief AspirinLow Dose 500 in 1 BOTTLE, PLASTIC TABLET, DELAYED RELEASE 500 19 11822-0600-6 Pain Relief AspirinLow Dose 1 in 1 CARTON TABLET, DELAYED RELEASE 1 19 11822-0600-6 Pain Relief AspirinLow Dose 200 in 1 BOTTLE, PLASTIC TABLET, DELAYED RELEASE 200 19 11822-0600-7 Pain Relief AspirinLow Dose 300 in 1 BOTTLE, PLASTIC TABLET, DELAYED RELEASE 300 19
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded ASPIRIN ACTIVE INGREDIENT R16CO5Y76E PAIN RELIEF ASPIRIN LOW DOSE (ASPIRIN) TABLET, COATED [RITE AID] 3 ASPIRIN ACTIVE MOIETY R16CO5Y76E PAIN RELIEF ASPIRIN LOW DOSE (ASPIRIN) TABLET, COATED [RITE AID] 3 CELLULOSE, MICROCRYSTALLINE INACTIVE INGREDIENT OP1R32D61U PAIN RELIEF ASPIRIN LOW DOSE (ASPIRIN) TABLET, COATED [RITE AID] 3 D&C YELLOW NO. 10 INACTIVE INGREDIENT 35SW5USQ3G PAIN RELIEF ASPIRIN LOW DOSE (ASPIRIN) TABLET, COATED [RITE AID] 3 HYPROMELLOSES INACTIVE INGREDIENT 3NXW29V3WO PAIN RELIEF ASPIRIN LOW DOSE (ASPIRIN) TABLET, COATED [RITE AID] 3 METHACRYLIC ACID INACTIVE INGREDIENT 1CS02G8656 PAIN RELIEF ASPIRIN LOW DOSE (ASPIRIN) TABLET, COATED [RITE AID] 3 POLYDEXTROSE INACTIVE INGREDIENT VH2XOU12IE PAIN RELIEF ASPIRIN LOW DOSE (ASPIRIN) TABLET, COATED [RITE AID] 3 POLYETHYLENE GLYCOLS INACTIVE INGREDIENT 3WJQ0SDW1A PAIN RELIEF ASPIRIN LOW DOSE (ASPIRIN) TABLET, COATED [RITE AID] 3 SHELLAC INACTIVE INGREDIENT 46N107B71O PAIN RELIEF ASPIRIN LOW DOSE (ASPIRIN) TABLET, COATED [RITE AID] 3 SODIUM BICARBONATE INACTIVE INGREDIENT 8MDF5V39QO PAIN RELIEF ASPIRIN LOW DOSE (ASPIRIN) TABLET, COATED [RITE AID] 3 SODIUM LAURYL SULFATE INACTIVE INGREDIENT 368GB5141J PAIN RELIEF ASPIRIN LOW DOSE (ASPIRIN) TABLET, COATED [RITE AID] 3 STARCH, CORN INACTIVE INGREDIENT O8232NY3SJ PAIN RELIEF ASPIRIN LOW DOSE (ASPIRIN) TABLET, COATED [RITE AID] 3 TALC INACTIVE INGREDIENT 7SEV7J4R1U PAIN RELIEF ASPIRIN LOW DOSE (ASPIRIN) TABLET, COATED [RITE AID] 3 TITANIUM DIOXIDE INACTIVE INGREDIENT 15FIX9V2JP PAIN RELIEF ASPIRIN LOW DOSE (ASPIRIN) TABLET, COATED [RITE AID] 3 TRIETHYL CITRATE INACTIVE INGREDIENT 8Z96QXD6UM PAIN RELIEF ASPIRIN LOW DOSE (ASPIRIN) TABLET, COATED [RITE AID] 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 11822-0600 PAIN RELIEF ASPIRIN LOW DOSE (ASPIRIN) TABLET, DELAYED RELEASE [RITE AID CORPORATION] 18 Current NDC, Legacy NDC, 8 package rows 20250502_503408ed-e799-48a0-8d38-3034f4a0ead5.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 56 of 79 · 1,576 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Quality Choice Effervescent Antacid and Pain Relief ASPIRIN, CITRIC ACID, SODIUM BICARBONATE Chain Drug Marketing Association 70d265de-ff94-e0e4-e053-2a91aa0a962a 2024-11-13 Warnings Exact identifier application number: M013 Quality Choice Extra Strength Effervescent Antacid and Pain Relief ASPIRIN, ANHYDROUS CITRIC ACID, SODIUM BICARBONATE Chain Drug Marketing Association 9f7d0c96-a561-a8a0-e053-2995a90a250b 2024-11-13 Warnings Exact identifier application number: M013 WinCo Foods Effervescent Antacid and Pain Relief ASPIRIN, SODIUM BICARBONATE, CITRIC ACID TABLET WinCo Foods, LLC 0c8a755a-089f-477f-97e9-0dd6fdfbe99d 2024-11-13 Warnings Exact identifier application number: M013 Acetaminophen ACETAMINOPHEN Kroger Company 8fb19444-f0e0-4d26-81e8-6a4b835056d8 2024-11-12 Warnings Exact identifier application number: M013 equate pain reliever ACETAMINOPHEN WALMART INC. 59d01f72-4575-48e2-b914-b6a6456ca7d2 2024-11-11 Warnings Exact identifier application number: M013 pain and fever ACETAMINOPHEN Kroger Company d181560c-1c39-4f2e-8a17-996224ca040f 2024-11-09 Warnings Exact identifier application number: M013 Childrens Tylenol ACETAMINOPHEN Kenvue Brands LLC babcb210-6a47-46ef-b4ea-bdde80411cd3 2024-11-08 Warnings Exact identifier application number: M013 Bayer Genuine Aspirin ASPIRIN Acme United Corporation f7f9dc46-a945-7ae3-e053-6394a90a1192 2024-11-08 Warnings Exact identifier application number: M013 TYLENOL Extra Strength ACETAMINOPHEN Kenvue Brands LLC dd87e342-b0cb-4111-9f15-415dbcda4b77 2024-11-07 Warnings Exact identifier application number: M013 Tylenol Extra Strength ACETAMINOPHEN Kenvue Brands LLC 0c5fdda8-5049-46de-e063-6294a90a592b 2024-11-07 Warnings Exact identifier application number: M013 Childrens TYLENOL ACETAMINOPHEN Kenvue Brands LLC 46ddbfde-54ab-4373-b832-b9c0620b1e9d 2024-11-07 Warnings Exact identifier application number: M013 Childrens TYLENOL ACETAMINOPHEN Kenvue Brands LLC 333f6231-3778-4c1f-9558-2afddca22c86 2024-11-07 Warnings Exact identifier application number: M013 Childrens TYLENOL ACETAMINOPHEN Kenvue Brands LLC 34247a3b-0846-4086-becd-76e630b3b721 2024-11-07 Warnings Exact identifier application number: M013 Childrens TYLENOL ACETAMINOPHEN Kenvue Brands LLC a51c2deb-c703-4dc8-9255-8ac9fe635170 2024-11-07 Warnings Exact identifier application number: M013 Childrens TYLENOL ACETAMINOPHEN Kenvue Brands LLC ce0a1fbc-7345-462b-b0da-c7149bdc288c 2024-11-07 Warnings Exact identifier application number: M013 TYLENOL Extra Strength ACETAMINOPHEN Kenvue Brands LLC 015a6179-bacb-452d-b594-4de628ddc11d 2024-11-07 Warnings Exact identifier application number: M013 TYLENOL Regular Strength ACETAMINOPHEN Kenvue Brands LLC de5c6654-56c5-40d3-a286-f04ed47ac7c8 2024-11-07 Warnings Exact identifier application number: M013 Midol Complete ACETAMINOPHEN, CAFFEINE, AND PYRILAMINE MALEATE Acme United Corporation f7bf126d-a6f1-231a-e053-6294a90a04e1 2024-11-07 Warnings Exact identifier application number: M013 CareOne Childrens Acetaminophen ACETAMINOPHEN American Sales Company 49021ae8-9655-4885-9f74-52df4cdcb26f 2024-11-07 Warnings Exact identifier application number: M013 aspirin ASPIRIN A-S Medication Solutions 65c41c20-2f9c-4012-900b-c2ffdf665144 2024-11-06 Warnings Exact identifier application number: M013
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 11822-0600-2 11822060002 1 BOTTLE, PLASTIC in 1 CARTON (11822-0600-2) / 32 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC 2023-03-01 No No Current 11822-0600-3 11822060003 1 BOTTLE, PLASTIC in 1 CARTON (11822-0600-3) / 120 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC 2008-02-12 0000-00-00 No No Current 11822-0600-4 11822060004 500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (11822-0600-4) 2008-02-12 0000-00-00 No No Current 11822-0600-6 11822060006 1 BOTTLE, PLASTIC in 1 CARTON (11822-0600-6) / 200 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC 2008-02-12 0000-00-00 No No Current 11822-0600-7 11822060007 300 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (11822-0600-7) 2008-02-12 0000-00-00 No No Current