FDA.reportPublic FDA data

Pain Relief Aspirin

Product NDC
11822-0157
11-digit product format
118220157
Labeler code
11822
Product ID
11822-0157_167acdfe-f258-43f2-a4e5-97e664133b4a
Type
HUMAN OTC DRUG
Nonproprietary name
Aspirin
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Rite Aid Corporation
Application
M013
Marketing category
OTC MONOGRAPH DRUG
Marketing start
1996-02-10
Substance
ASPIRIN
Active strength
325 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
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Pain Relief Aspirin
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ASPIRIN325 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiR16CO5Y76E
Rxcui212033

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
d7724692-1155-4cc8-a415-22f5fc4aec35Product name620220216
bde672ba-4805-28d0-1986-73543d41b412Product name220210201
f212291f-05fe-9603-fc7e-bd73e38ce1e6Product name220161129
ade821ba-260a-47e2-bd89-743e27ac9906Product name120161121
182f9ab4-4ab5-c449-200f-87ce2ce8e550Product name220151105
9425d234-4ae1-4b53-adc6-8cc7af6dd657Product name120150929
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
11822-0157-2Pain Relief Aspirin100 in 1 BOTTLE, PLASTICTABLET, FILM COATED10017
11822-0157-3Pain Relief Aspirin250 in 1 BOTTLE, PLASTICTABLET, FILM COATED25017
11822-0157-4Pain Relief Aspirin500 in 1 BOTTLE, PLASTICTABLET, FILM COATED50017

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ASPIRINACTIVE INGREDIENTR16CO5Y76EPAIN RELIEF ASPIRIN (ASPIRIN) TABLET [RITE AID]3
ASPIRINACTIVE MOIETYR16CO5Y76EPAIN RELIEF ASPIRIN (ASPIRIN) TABLET [RITE AID]3
HYPROMELLOSESINACTIVE INGREDIENT3NXW29V3WOPAIN RELIEF ASPIRIN (ASPIRIN) TABLET [RITE AID]3
POLYETHYLENE GLYCOLSINACTIVE INGREDIENT3WJQ0SDW1APAIN RELIEF ASPIRIN (ASPIRIN) TABLET [RITE AID]3
PROPYLENE GLYCOLINACTIVE INGREDIENT6DC9Q167V3PAIN RELIEF ASPIRIN (ASPIRIN) TABLET [RITE AID]3
STARCH, CORNINACTIVE INGREDIENTO8232NY3SJPAIN RELIEF ASPIRIN (ASPIRIN) TABLET [RITE AID]3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11822-0157PAIN RELIEF ASPIRIN (ASPIRIN) TABLET, FILM COATED [RITE AID CORPORATION]16Current NDC, Legacy NDC, 3 package rows20240623_bd69d3d2-5d38-47c6-98a6-124f7a43b8b0.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
212033aspirin 325 MG Oral TabletPSNbd69d3d2-5d38-47c6-98a6-124f7a43b8b017
212033aspirin 325 MG Oral TabletSCDbd69d3d2-5d38-47c6-98a6-124f7a43b8b017
212033ASA 325 MG Oral TabletSYbd69d3d2-5d38-47c6-98a6-124f7a43b8b017

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
11822-0157-211822015702100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (11822-0157-2) 1996-02-100000-00-00NoNoCurrent
11822-0157-311822015703250 TABLET, FILM COATED in 1 BOTTLE (11822-0157-3) 1996-02-100000-00-00NoNoCurrent
11822-0157-411822015704500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (11822-0157-4) 1996-02-100000-00-00NoNoCurrent