Acetaminophen PM

Product NDC
69842-956
11-digit product format
698420956
Labeler code
69842
Product ID
69842-956_47ca6770-e94f-4ccf-ac53-ddbccfd93d22
Type
HUMAN OTC DRUG
Nonproprietary name
Acetaminophen, Diphenhydramine HCl
Dosage form
TABLET, COATED
Route
ORAL
Labeler
CVS PHARMACY
Application
M013
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2007-12-17
Substance
ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE
Active strength
500; 25 mg/1; mg/1
Pharmacologic classes
Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
NDC exclude flag
No
Listing certified through
2027-12-31
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 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage69842-95669842-956-09DDiscontinued by firm2026-10-27
excluded packagepackage69842-95669842-956-13DDiscontinued by firm2026-10-27

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 · 24 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 2025-12-0569842-956-13d630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-0569842-956-09d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-2669842-956-13f5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-2669842-956-09f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-3169842-956-132ef7874e63bc…57b86245f4fa…
2025-04-01 02:39 UTC · source 2025-03-3169842-956-092ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-2869842-956-13a1b67e2a42f9…c4cf2c586c0d…
2025-03-28 20:22 UTC · source 2025-03-2869842-956-09a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-2169842-956-13cfe11265f3b6…090c488252e2…
2025-03-22 03:12 UTC · source 2025-03-2169842-956-09cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-1069842-956-13cdf11ea48f46…ba0047e9e063…
2025-03-10 12:48 UTC · source 2025-03-1069842-956-09cdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-3169842-956-13302b2466d912…e7b80fea0513…
2025-02-02 03:52 UTC · source 2025-01-3169842-956-09302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-2069842-956-13ed331223b511…672a5bd82f5f…
2025-01-20 13:05 UTC · source 2025-01-2069842-956-09ed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-1069842-956-130efc9e666f02…f202fb6c5f17…
2025-01-11 03:41 UTC · source 2025-01-1069842-956-090efc9e666f02…f202fb6c5f17…
2024-11-09 02:27 UTC · source 2024-11-0869842-956-13ad56d346431e…cc804d4bbf1e…
2024-11-09 02:27 UTC · source 2024-11-0869842-956-09ad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-0369842-956-13367a005e9d99…383a685ebd0f…
2024-10-04 04:10 UTC · source 2024-10-0369842-956-09367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-0969842-956-09557ba5c1ecfa…9c80585c8c6e…
2024-07-10 04:00 UTC · source 2024-07-0969842-956-13557ba5c1ecfa…9c80585c8c6e…

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
Acetaminophen PM
Brand name suffix
Extra Strength
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ACETAMINOPHEN500 mg/1
DIPHENHYDRAMINE HYDROCHLORIDE25 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
362O9ITL9DInternal UNII lookup
TC2D6JAD40Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1092189Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
67a190c3-7de0-4f57-be94-d6b8285e1220Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0e2e0f88-b076-afe1-4bdd-32bca4375becProduct name320250127
3e48c9c4-918d-5d23-2f0b-d2398b06be54Product name120140508
865c72dd-0d94-daac-f728-ddd4ded2a79eProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69842-956-09Acetaminophen PMExtra Strength1 in 1 CARTONTABLET, COATED112
69842-956-09Acetaminophen PMExtra Strength20 in 1 BOTTLE, PLASTICTABLET, COATED2012
69842-956-13Acetaminophen PMExtra Strength250 in 1 BOTTLETABLET, COATED25012
69842-956-31Acetaminophen PMExtra Strength80 in 1 BOTTLE, PLASTICTABLET, COATED8012

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69842-956ACETAMINOPHEN PM EXTRA STRENGTH (ACETAMINOPHEN, DIPHENHYDRAMINE HCL) TABLET, COATED [CVS PHARMACY]11Current NDC, Legacy NDC, 4 package rows20250327_67a190c3-7de0-4f57-be94-d6b8285e1220.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 77 of 79 · 1,561 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ExtraprinACETAMINOPHEN, ASPIRIN, CAFFEINEMagno-Humphries, Inc.9d22cdc8-29c5-4273-e053-2a95a90ad0bf2023-10-27WarningsExact identifier
application number: M013
Regular Strength Enteric coated aspirinASPIRINGeri-Care Pharmaceutical Corpc321208c-f192-42c5-9454-e0df5d02d6852023-10-26WarningsExact identifier
application number: M013
Pain RelieverACETAMINOPHENWALGREENSf3c69974-7f51-2227-e053-2995a90a55702023-10-21WarningsExact identifier
application number: M013
Menstrual CompleteMENSTRUAL COMPLETEHealthlife of USAc7e89b01-a8eb-4487-8f0b-a4b9ae6d9f332023-10-21WarningsExact identifier
application number: M013
Extra Strength Pain ReliefACETAMINOPHENGeri-Care Pharmaceutical Corpe65dbd01-2d5e-4067-ad98-98d879cfb5ee2023-10-19WarningsExact identifier
application number: M013
Regular Strength Pain RelieverACETAMINOPHENINGLES MARKETS, INC.f06fe167-8a16-14d9-e053-2a95a90a1a0f2023-10-17WarningsExact identifier
application number: M013
Childrens Chewable AcetaminophenACETAMINOPHENBLESSINGS INTERNATIONALee8ba190-2c42-7ca2-e053-2a95a90a01a02023-10-17WarningsExact identifier
application number: M013
AphenACETAMINOPHENAsclemed USA, Inc.fe3c0a2b-316b-4620-b6bc-378dbaf7ed572023-10-16WarningsExact identifier
application number: M013
Pain Reliever Extra StrengthACETAMINOPHENWalgreensb4b06d32-6a09-4c43-980b-377b617ba7392023-10-09WarningsExact identifier
application number: M013
FLO PMS CompleteACETAMINOPHEN, CAFFEINE, PYRILAMINE MALEATEO Positiv, Inc.cce62d9f-adb1-4473-8258-910dff6b13782023-10-09WarningsExact identifier
application number: M013
childrens mapapACETAMINOPHENProficient Rx LP88c4183a-3032-46de-bf18-f700055f617b2023-10-01WarningsExact identifier
application number: M013
Tri-Buffered AspirinASPIRINProficient Rx LP640c3311-2abf-40b2-82b9-9fe4d8c1cf1d2023-10-01WarningsExact identifier
application number: M013
AcetaminophenACETAMINOPHENCVS PHARMACY, INC852e70e2-7279-6f33-e053-2991aa0a86762023-08-28WarningsExact identifier
application number: M013
Children Pain ReliefCHILDREN PAIN RELIEFAllegiant Health44c90cbe-8ece-4dd8-9ea5-7f8d6f4c00962023-07-17WarningsExact identifier
application number: M013
Aspirin Low DoseASPIRINBetter Living Brands LLC4a76e898-3204-4f77-bc67-c19f5fe829f32023-07-05WarningsExact identifier
application number: M013
Aspirin Enteric CoatedASPIRIN 81 MGLodaat LLC04017bc9-602a-4204-96a9-b7f9713155f62023-01-31WarningsExact identifier
application number: M013
Aspirin 325 mgASPIRINWALGREENSd71a22e8-9e39-a672-e053-2a95a90a14032022-07-08WarningsExact identifier
application number: M013
Pain Relief Extra StrengthPAIN RELIEFAllegiant Healthd41d2319-8eed-4df9-813c-313497ceb8b42021-11-23WarningsExact identifier
application number: M013
Pain Relief PM Extra StrengthPAIN RELIEF PMAllegiant Health4c9969be-a01f-4ca4-800a-e404229ce28b2021-11-23WarningsExact identifier
application number: M013
Tension Headache ReliefTENSION HEADACHE RELIEFAllegiant Health9d348550-060b-410f-8c1e-8f43d00b860e2021-11-22WarningsExact identifier
application number: M013

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1092189acetaminophen 500 MG / diphenhydrAMINE HCl 25 MG Oral TabletPSN67a190c3-7de0-4f57-be94-d6b8285e122012
1092189acetaminophen 500 MG / diphenhydramine hydrochloride 25 MG Oral TabletSCD67a190c3-7de0-4f57-be94-d6b8285e122012
1092189APAP 500 MG / diphenhydramine hydrochloride 25 MG Oral TabletSY67a190c3-7de0-4f57-be94-d6b8285e122012

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
69842-956-09698420956091 BOTTLE, PLASTIC in 1 CARTON (69842-956-09) > 20 TABLET in 1 BOTTLE, PLASTIC2007-12-170000-00-00NoNoCurrent
69842-956-1369842095613250 in 1 BOTTLEHistorical
69842-956-316984209563180 TABLET, COATED in 1 BOTTLE, PLASTIC (69842-956-31) 2007-12-170000-00-00NoNoCurrent