Pain Relief

Product NDC
53943-304
11-digit product format
539430304
Labeler code
53943
Product ID
53943-304_288998e3-a490-9c47-e063-6394a90ae9aa
Type
HUMAN OTC DRUG
Nonproprietary name
Acetaminophen
Dosage form
TABLET, COATED
Route
ORAL
Labeler
DISCOUNT DRUG MART
Application
M013
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2010-01-05
Substance
ACETAMINOPHEN
Active strength
500 mg/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 3 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage53943-30453943-304-02DDiscontinued by firm2026-10-21
excluded packagepackage53943-30453943-304-04DDiscontinued by firm2026-10-21
excluded packagepackage53943-30453943-304-09DDiscontinued by firm2026-10-21

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 1 · 18 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Package NDC, Snapshot table
Captured / source datePackage NDCSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-0553943-304-04d630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-0553943-304-02d630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-0553943-304-09d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-2653943-304-04f5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-2653943-304-02f5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-2653943-304-09f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-3153943-304-042ef7874e63bc…57b86245f4fa…
2025-04-01 02:39 UTC · source 2025-03-3153943-304-022ef7874e63bc…57b86245f4fa…
2025-04-01 02:39 UTC · source 2025-03-3153943-304-092ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-2853943-304-04a1b67e2a42f9…c4cf2c586c0d…
2025-03-28 20:22 UTC · source 2025-03-2853943-304-02a1b67e2a42f9…c4cf2c586c0d…
2025-03-28 20:22 UTC · source 2025-03-2853943-304-09a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-2153943-304-04cfe11265f3b6…090c488252e2…
2025-03-22 03:12 UTC · source 2025-03-2153943-304-02cfe11265f3b6…090c488252e2…
2025-03-22 03:12 UTC · source 2025-03-2153943-304-09cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-1053943-304-04cdf11ea48f46…ba0047e9e063…
2025-03-10 12:48 UTC · source 2025-03-1053943-304-02cdf11ea48f46…ba0047e9e063…
2025-03-10 12:48 UTC · source 2025-03-1053943-304-09cdf11ea48f46…ba0047e9e063…

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
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ACETAMINOPHEN500 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
362O9ITL9DInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
198440Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
972f09a7-2aa1-4b1b-a6dc-2c4578a07803Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
53943-304-02Pain Relief50 in 1 BOTTLE, PLASTICTABLET, COATED505
53943-304-02Pain Relief1 in 1 CARTONTABLET, COATED15
53943-304-04Pain Relief1 in 1 CARTONTABLET, COATED15
53943-304-04Pain Relief100 in 1 BOTTLE, PLASTICTABLET, COATED1005
53943-304-06Pain Relief500 in 1 BOTTLE, PLASTICTABLET, COATED5005
53943-304-09Pain Relief100 in 1 BOTTLE, PLASTICTABLET, COATED1005
53943-304-09Pain Relief2 in 1 CARTONTABLET, COATED25

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
53943-304PAIN RELIEF (ACETAMINOPHEN) TABLET, COATED [DISCOUNT DRUG MART]5Current NDC, Legacy NDC, 7 package rows20241208_972f09a7-2aa1-4b1b-a6dc-2c4578a07803.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 · 1,579 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Cabinet Pain Reliever and Fever Reducer Refill AcetaminophenACETAMINOPHENCabinet Health P.B.C.2744f082-adfd-4dfc-a87d-ed8c0d84a4472025-10-01WarningsExact identifier
application number: M013
ASPIRINASPIRINMarc Glassman, Inc.14cb1d2d-95b8-447e-8d79-e6ec82c0e4312025-10-01WarningsExact identifier
application number: M013
ACETAMINOPHEN 325 MGACETAMINOPHENProficient Rx LP6794830a-7856-464d-84be-c8b253cf41ac2025-10-01WarningsExact identifier
application number: M013
Enteric Coated Aspirin Regular StrengthASPIRINBryant Ranch Prepacke05140fa-9766-4f97-bffc-e36a01b9d38f2025-10-01WarningsExact identifier
application number: M013
Acetaminophen gelcapsACETAMINOPHENTARGET CORPORATION2ea1931e-334e-a551-e063-6394a90a03b92025-09-29WarningsExact identifier
application number: M013
acetaminophenACETAMINOPHENTARGET CORPORATION8ed1d1f5-fe4a-5fd8-e053-2a95a90a90fb2025-09-29WarningsExact identifier
application number: M013
Pain Relief PM Extra StrengthACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDETopCo Associates LLC3b672ec7-8658-4b43-a79d-094ac8bc69042025-09-29WarningsExact identifier
application number: M013
kirkland signature acetaminophen adult extra strengthACETAMINOPHENCostco Wholesale Companya9979167-1a82-47d7-9602-2865f9bdd6282025-09-27WarningsExact identifier
application number: M013
First Aid Direct Chewable AspirinASPIRINCintas Corpff6960f6-9f55-4f32-9ab5-9187724531e92025-09-25WarningsExact identifier
application number: M013
Bayer Rapid Relief Body PainASPIRIN/CAFFEINE ORAL POWDERBayer HealthCare LLC.3fa1ec07-d1a6-226b-e063-6394a90a32132025-09-25WarningsExact identifier
application number: M013
Xpect Chewable AspirinASPIRINCintas Corporationbddce374-1d35-4685-987d-4a4cc99941552025-09-25WarningsExact identifier
application number: M013
IBUPROFENIBUPROFENKroger Companybbedfc37-913d-8046-e053-2995a90af68a2025-09-24WarningsExact identifier
application number: M013
Xpect Pain Away Extra StrengthACETAMINOPHEN ASPIRIN CAFFEINECintas Corporation1269d069-afaf-4ca5-b369-f74249a348db2025-09-24WarningsExact identifier
application number: M013
Aspirin Low DoseASPIRINPreferred Pharmaceuticals Inc.29214eec-860c-43f0-83c6-9ed5a9f530af2025-09-22WarningsExact identifier
application number: M013
ASPIRINASPIRINKroger Companybbee8ee4-e09d-3ba6-e053-2a95a90af6472025-09-19WarningsExact identifier
application number: M013
careone acetaminophenACETAMINOPHENAmerican Sales Company4bb696f6-a47b-4da9-9224-9aeae3e152f32025-09-19WarningsExact identifier
application number: M013
Childrens Pain ReliefACETAMINOPHENAurohealth LLC49a740ec-8ed4-4c76-b2d0-c13651bafa5e2025-09-18WarningsExact identifier
application number: M013
Extra Strength Headache ReliefACETAMINOPHEN, ASPIRIN, AND CAFFEINEAdvanced Rx LLCa7ed4c76-a5b5-44f7-866f-f43790e45c782025-09-18WarningsExact identifier
application number: M013
acetaminophenACETAMINOPHENCVS Pharmacyfc2d4367-8884-4b76-aa3e-8c35be1ace492025-09-18WarningsExact identifier
application number: M013
Aspirin Enteric Coated, Regular StrengthASPIRINWalgreen Company5e1484d3-5be1-40da-a3bf-fb19f7d27d452025-09-18WarningsExact identifier
application number: M013

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
198440acetaminophen 500 MG Oral TabletPSN972f09a7-2aa1-4b1b-a6dc-2c4578a078035
198440acetaminophen 500 MG Oral TabletSCD972f09a7-2aa1-4b1b-a6dc-2c4578a078035
198440APAP 500 MG Oral TabletSY972f09a7-2aa1-4b1b-a6dc-2c4578a078035

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
53943-304-02539430304021 BOTTLE, PLASTIC in 1 CARTON (53943-304-02) > 50 TABLET, COATED in 1 BOTTLE, PLASTIC2010-01-050000-00-00NoNoCurrent
53943-304-04539430304041 BOTTLE, PLASTIC in 1 CARTON (53943-304-04) > 100 TABLET, COATED in 1 BOTTLE, PLASTIC2010-03-040000-00-00NoNoCurrent
53943-304-0653943030406500 TABLET, COATED in 1 BOTTLE, PLASTIC (53943-304-06) 2010-01-050000-00-00NoNoCurrent
53943-304-09539430304092 BOTTLE, PLASTIC in 1 CARTON (53943-304-09) > 100 TABLET, COATED in 1 BOTTLE, PLASTIC2013-04-040000-00-00NoNoCurrent