FDA.reportPublic FDA data

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
IngredientStrength
ASPIRIN81 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
R16CO5Y76EInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
308416Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
503408ed-e799-48a0-8d38-3034f4a0ead5Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
fb7ab793-2c12-4079-b100-a64f73bef25aProduct name420240712
b0cbf770-6cc3-4aa4-9158-755110c2b9f7Product name220230717
dc7c5daa-021f-40dd-b00d-63982cb2067aProduct name120230426
d7724692-1155-4cc8-a415-22f5fc4aec35Product name620220216
bde672ba-4805-28d0-1986-73543d41b412Product name220210201
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name520200925
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
f212291f-05fe-9603-fc7e-bd73e38ce1e6Product name220161129
ade821ba-260a-47e2-bd89-743e27ac9906Product name120161121
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name220160823
182f9ab4-4ab5-c449-200f-87ce2ce8e550Product name220151105
9425d234-4ae1-4b53-adc6-8cc7af6dd657Product name120150929
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
2a21311a-89e2-0e83-2ebd-117f9798b2b2Product name120140508
9007e8a7-ff50-f9b9-7945-f2a1deadd94eProduct name120140508
96c2be53-8e44-452d-56a2-d255b2f1af2dProduct name120140508
bf8bd5f7-495f-4022-2780-7ded7ea7ea44Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11822-0600-2Pain Relief AspirinLow Dose1 in 1 CARTONTABLET, DELAYED RELEASE119
11822-0600-2Pain Relief AspirinLow Dose32 in 1 BOTTLE, PLASTICTABLET, DELAYED RELEASE3219
11822-0600-3Pain Relief AspirinLow Dose120 in 1 BOTTLE, PLASTICTABLET, DELAYED RELEASE12019
11822-0600-3Pain Relief AspirinLow Dose1 in 1 CARTONTABLET, DELAYED RELEASE119
11822-0600-4Pain Relief AspirinLow Dose500 in 1 BOTTLE, PLASTICTABLET, DELAYED RELEASE50019
11822-0600-6Pain Relief AspirinLow Dose1 in 1 CARTONTABLET, DELAYED RELEASE119
11822-0600-6Pain Relief AspirinLow Dose200 in 1 BOTTLE, PLASTICTABLET, DELAYED RELEASE20019
11822-0600-7Pain Relief AspirinLow Dose300 in 1 BOTTLE, PLASTICTABLET, DELAYED RELEASE30019

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ASPIRINACTIVE INGREDIENTR16CO5Y76EPAIN RELIEF ASPIRIN LOW DOSE (ASPIRIN) TABLET, COATED [RITE AID]3
ASPIRINACTIVE MOIETYR16CO5Y76EPAIN RELIEF ASPIRIN LOW DOSE (ASPIRIN) TABLET, COATED [RITE AID]3
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UPAIN RELIEF ASPIRIN LOW DOSE (ASPIRIN) TABLET, COATED [RITE AID]3
D&C YELLOW NO. 10INACTIVE INGREDIENT35SW5USQ3GPAIN RELIEF ASPIRIN LOW DOSE (ASPIRIN) TABLET, COATED [RITE AID]3
HYPROMELLOSESINACTIVE INGREDIENT3NXW29V3WOPAIN RELIEF ASPIRIN LOW DOSE (ASPIRIN) TABLET, COATED [RITE AID]3
METHACRYLIC ACIDINACTIVE INGREDIENT1CS02G8656PAIN RELIEF ASPIRIN LOW DOSE (ASPIRIN) TABLET, COATED [RITE AID]3
POLYDEXTROSEINACTIVE INGREDIENTVH2XOU12IEPAIN RELIEF ASPIRIN LOW DOSE (ASPIRIN) TABLET, COATED [RITE AID]3
POLYETHYLENE GLYCOLSINACTIVE INGREDIENT3WJQ0SDW1APAIN RELIEF ASPIRIN LOW DOSE (ASPIRIN) TABLET, COATED [RITE AID]3
SHELLACINACTIVE INGREDIENT46N107B71OPAIN RELIEF ASPIRIN LOW DOSE (ASPIRIN) TABLET, COATED [RITE AID]3
SODIUM BICARBONATEINACTIVE INGREDIENT8MDF5V39QOPAIN RELIEF ASPIRIN LOW DOSE (ASPIRIN) TABLET, COATED [RITE AID]3
SODIUM LAURYL SULFATEINACTIVE INGREDIENT368GB5141JPAIN RELIEF ASPIRIN LOW DOSE (ASPIRIN) TABLET, COATED [RITE AID]3
STARCH, CORNINACTIVE INGREDIENTO8232NY3SJPAIN RELIEF ASPIRIN LOW DOSE (ASPIRIN) TABLET, COATED [RITE AID]3
TALCINACTIVE INGREDIENT7SEV7J4R1UPAIN RELIEF ASPIRIN LOW DOSE (ASPIRIN) TABLET, COATED [RITE AID]3
TITANIUM DIOXIDEINACTIVE INGREDIENT15FIX9V2JPPAIN RELIEF ASPIRIN LOW DOSE (ASPIRIN) TABLET, COATED [RITE AID]3
TRIETHYL CITRATEINACTIVE INGREDIENT8Z96QXD6UMPAIN RELIEF ASPIRIN LOW DOSE (ASPIRIN) TABLET, COATED [RITE AID]3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11822-0600PAIN RELIEF ASPIRIN LOW DOSE (ASPIRIN) TABLET, DELAYED RELEASE [RITE AID CORPORATION]18Current NDC, Legacy NDC, 8 package rows20250502_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 72 of 79 · 1,570 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Dolex Children Pain and FeverACETAMINOPHENPharmadel LLCf9158463-aeb1-5de0-e053-6294a90a748b2024-03-04WarningsExact identifier
application number: M013
SEDALMEX FORTEACETAMINOPHEN, ASPIRIN, CAFFEINEBelmora LLC33b3508e-4caa-4d05-9b15-cb82a2ee2d4d2024-02-28WarningsExact identifier
application number: M013
Pain ReliefACETAMINOPHENAMERISOURCE BERGEN2b923a97-836c-4dac-a8c0-3047a35fb62e2024-02-23WarningsExact identifier
application number: M013
Pain Reliever PM Extra StrengthACETAMINOPHEN, DIPHENHYDRAMINE HCLBJWC (Berkley & Jensen / BJ's)b20a08f3-c9c0-4bd9-8ce0-acb932b5bb862024-02-22WarningsExact identifier
application number: M013
M-PAPACETAMINOPHENBryant Ranch Prepack31a41976-7f65-42d7-acf5-de9c2c5ca58e2024-02-20WarningsExact identifier
application number: M013
Publix Fast Relief Effervescent - Original FlavorASPIRINPUBLIX SUPER MARKETS INC.0a342f72-45fd-3e12-e063-6394a90ae33e2024-02-16WarningsExact identifier
application number: M013
Equaline Effervescent Pain RelieverASPIRINUNITED NATURAL FOODS, INC. DBA UNFI0761299a-e913-7665-e063-6394a90a60032024-02-16WarningsExact identifier
application number: M013
TopCare Effervescent Pain ReliefASPIRINTOPCO ASSOCIATES LLC075f36e1-110c-e839-e063-6294a90a89d72024-02-16WarningsExact identifier
application number: M013
Extra Strength Pain RelieverACETAMINOPHENINGLES MARKETS, INC.115d0b4f-6f0f-79a9-e063-6394a90ab18a2024-02-14WarningsExact identifier
application number: M013
PANADOLACETAMINOPHENHaleon US Holdings LLCe1799765-c247-42b4-ad6a-8ba7d136abf22024-02-06WarningsExact identifier
application number: M013
Panadol Cold and Flu NonDrowsyACETAMINOPHEN AND PHENYLEPRINE HCLHaleon US Holdings LLCf626ab17-01c9-4493-ba9e-0c8c111463842024-02-06WarningsExact identifier
application number: M013
PANADOL ExtraACETAMINOPHEN AND CAFFEINEHaleon US Holdings LLCe5c2d88a-d903-4ca0-b895-f27e791dfc4e2024-02-06WarningsExact identifier
application number: M013
PANADOL Extra StrengthACETAMINOPHENHaleon US Holdings LLCb2fe7f47-1a2e-40ee-8f8f-38f2028dce1b2024-02-06WarningsExact identifier
application number: M013
PANADOL Extra StrengthACETAMINOPHENHaleon US Holdings LLC9d384e88-5c11-4600-ac6c-a383715701382024-02-06WarningsExact identifier
application number: M013
PANADOLACETAMINOPHENHaleon US Holdings LLC95801755-db54-4ad7-bec1-52671914f6ca2024-02-06WarningsExact identifier
application number: M013
PANADOL PMACETAMINOPHEN AND DIPHENHYDRAMINE HCLHaleon US Holdings LLC01e7dddb-755c-4745-b701-edcdb62090642024-02-06Warnings, Adverse reactionsExact identifier
application number: M013
PANADOL PMACETAMINOPHEN AND DIPHENHYDRAMINE HCLHaleon US Holdings LLCfe7cd1f2-9b00-4ded-99c2-8a152c71093c2024-02-06Warnings, Adverse reactionsExact identifier
application number: M013
Childrens Pain and FeverACETAMINOPHENAptaPharma Inc.9064943f-836f-4853-b6f2-2c4879941eeb2024-02-02WarningsExact identifier
application number: M013
Quality Choice Effervescent Pain ReliefASPIRINCHAIN DRUG MARKETING ASSOCIATION, INC.079af5d7-1be8-2a93-e063-6294a90a496d2024-02-01WarningsExact identifier
application number: M013
MEDI-FIRST Non-AspirinACETAMINOPHENProficient Rx LP4c84948d-3a95-4c53-8529-7e7b9d8bb6df2024-02-01WarningsExact identifier
application number: M013

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
308416aspirin 81 MG Delayed Release Oral TabletPSN503408ed-e799-48a0-8d38-3034f4a0ead519
308416aspirin 81 MG Delayed Release Oral TabletSCD503408ed-e799-48a0-8d38-3034f4a0ead519
308416ASA 81 MG Delayed Release Oral TabletSY503408ed-e799-48a0-8d38-3034f4a0ead519
308416aspirin 81 MG Enteric Coated Oral TabletSY503408ed-e799-48a0-8d38-3034f4a0ead519

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
11822-0600-2118220600021 BOTTLE, PLASTIC in 1 CARTON (11822-0600-2) / 32 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC2023-03-01NoNoCurrent
11822-0600-3118220600031 BOTTLE, PLASTIC in 1 CARTON (11822-0600-3) / 120 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC2008-02-120000-00-00NoNoCurrent
11822-0600-411822060004500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (11822-0600-4) 2008-02-120000-00-00NoNoCurrent
11822-0600-6118220600061 BOTTLE, PLASTIC in 1 CARTON (11822-0600-6) / 200 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC2008-02-120000-00-00NoNoCurrent
11822-0600-711822060007300 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (11822-0600-7) 2008-02-120000-00-00NoNoCurrent