FDA.reportPublic FDA data

Pain Relief

Product NDC
83324-081
11-digit product format
833240081
Labeler code
83324
Product ID
83324-081_1ac6e721-4d0a-0396-e063-6294a90a7fe9
Type
HUMAN OTC DRUG
Nonproprietary name
Acetaminophen
Dosage form
TABLET
Route
ORAL
Labeler
Chain Drug Marketing Association
Application
M013
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2024-04-26
Substance
ACETAMINOPHEN
Active strength
500 mg/1
NDC exclude flag
No
Listing certified through
2026-12-31
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
Brand name suffix
Extra Strength
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
cfaf9495-e654-4dfc-ba23-d2358c3720c4Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83324-081-01Pain ReliefExtra Strength100 in 1 PACKAGETABLET1002
83324-081-01Pain ReliefExtra Strength1 in 1 CARTONTABLET12
83324-081-10Pain ReliefExtra Strength100 in 1 BOTTLE, PLASTICTABLET1002
83324-081-60Pain ReliefExtra Strength60 in 1 BOTTLE, PLASTICTABLET602
83324-081-60Pain ReliefExtra Strength1 in 1 CARTONTABLET12

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
83324-081-01EA - Each83324-081e54beb91-3e2c-4ee4-93be-0ea7ee0c454a12026-01-08
83324-081-10EA - Each83324-0812b7a8e0d-06af-48b6-9c17-b2bd7bccc12112026-01-08

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83324-081PAIN RELIEF EXTRA STRENGTH (ACETAMINOPHEN) TABLET [CHAIN DRUG MARKETING ASSOCIATION]2Current NDC, 5 package rows20240615_cfaf9495-e654-4dfc-ba23-d2358c3720c4.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 52 of 79 · 1,570 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Acetaminophen 250mg Aspirin 250mg Caffeine 65mgACETAMINOPHEN 250MG ASPIRIN 250MG CAFFEINE 65MGCVS Pharmacyb9e5df0e-06d3-6f72-e053-2995a90a2d072024-12-14WarningsExact identifier
application number: M013
Alka-Seltzer Heartburn and PainANHYDROUS CITRIC ACID, ASPIRIN, AND SODIUM BICARBONATEBayer HealthCare LLC.2928e140-c868-5bf5-e063-6394a90ab0242024-12-13WarningsExact identifier
application number: M013
foster and thrive pain relieverACETAMINOPHENStrategic Sourcing Services LLCb8ee568c-80cf-4e35-865e-35516bdab0fd2024-12-13WarningsExact identifier
application number: M013
Headache ReliefACETAMINOPHEN, ASPIRIN, CAFFEINEStrive Pharmaceuticals Inc.c0de0bd2-4868-46dc-a20f-3ca02caaa26b2024-12-11WarningsExact identifier
application number: M013
Rite Aid Antacid and Pain ReliefASPIRIN, CITRIC ACID, SODIUM BICARBONATERite Aidb4797380-9cef-d640-e053-2a95a90a06652024-12-11WarningsExact identifier
application number: M013
Top Value Effervescent Pain ReliefASPIRIN, CITRIC ACID, SODIUM BICAROBONATETower Laboratories Ltd44babed8-cf38-1c12-e054-00144ff8d46c2024-12-11Warnings, Adverse reactionsExact identifier
application number: M013
Best Choice Effervescent Antacid Pain ReliefASPIRIN, CITRIC ACID, SODIUM BICARBONATEValu Merchandisers Companyb5e2300a-b77b-53cc-e053-2a95a90a7a6e2024-12-11WarningsExact identifier
application number: M013
EXTRA STRENGTH Headache Relief geltabsACETAMINOPHEN, ASPIRIN, CAFFEINEStrive Pharmaceuticals Inc.b432771a-4f7d-4d39-a038-d1561d8f67082024-12-11WarningsExact identifier
application number: M013
Pain Relief ChildrensACETAMINOPHENQUALITY CHOICE (Chain Drug Marketing Association)223ffb2b-3ee5-4118-955b-bc4fa4e8a2e62024-12-10WarningsExact identifier
application number: M013
acetaminophenACETAMINOPHENUNFIe689c9e3-dd4d-c646-e053-2a95a90a4b6a2024-12-09WarningsExact identifier
application number: M013
DrKids Childrens Pain and FeverACETAMINOPHEN 80MG/PIECECalmCo LLCff4b0528-39a0-80d5-e053-6394a90a8a832024-12-07WarningsExact identifier
application number: M013
Pain ReliefACETAMINOPHENDISCOUNT DRUG MART972f09a7-2aa1-4b1b-a6dc-2c4578a078032024-12-05WarningsExact identifier
application number: M013
Pain Relief Extra StrengthACETAMINOPHENDISCOUNT DRUG MARTe6feff0a-3347-194d-e053-2a95a90acd202024-12-05WarningsExact identifier
application number: M013
Pain Relief Extra StrengthACETAMINOPHENDISCOUNT DRUG MARTe6fee238-0b6f-cb84-e053-2995a90a361b2024-12-05WarningsExact identifier
application number: M013
Menstrual Complete Maximum StrengthACETAMINOPHEN, CAFFEINE AND PYRILAMINE MALEATEL.N.K. International, Inc.379ef03c-3b6a-40c3-b736-99f0537d26c82024-12-05WarningsExact identifier
application number: M013
Pain Reliever Extra StrengthACETAMINOPHENMarc Glassman, Inc.43bf297f-2832-424f-a013-4bfa1d6c03e62024-12-04WarningsExact identifier
application number: M013
AcetaminophenACETAMINOPHENPrecision Dose, Inc.5a68ab98-720c-479a-a60a-4e594add6c092024-12-04WarningsExact identifier
application number: M013
HEB Effervescent Pain ReliefASPIRINH. E. BUTT GROCERY COMPANY03876c71-60ec-3280-e063-6294a90a62dc2024-12-03WarningsExact identifier
application number: M013
Migrafein FORTEACETAMINOPHEN, CAFFEINEOPMX LLC028875c9-4129-ce2c-e063-6294a90a26cc2024-12-03WarningsExact identifier
application number: M013
Neo-Lubrina FuerteACETAMINOPHEN, CAFFEINEOPMX LLC0288a327-fd4b-1991-e063-6294a90ace502024-12-03WarningsExact identifier
application number: M013

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
198440acetaminophen 500 MG Oral TabletPSNcfaf9495-e654-4dfc-ba23-d2358c3720c42
198440acetaminophen 500 MG Oral TabletSCDcfaf9495-e654-4dfc-ba23-d2358c3720c42
198440APAP 500 MG Oral TabletSYcfaf9495-e654-4dfc-ba23-d2358c3720c42

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
83324-081-01833240081011 PACKAGE in 1 CARTON (83324-081-01) / 100 TABLET in 1 PACKAGE1 package2024-04-26NoNoCurrent
83324-081-1083324008110100 TABLET in 1 BOTTLE, PLASTIC (83324-081-10) 100 tablet2024-06-12NoNoCurrent
83324-081-60833240081601 BOTTLE, PLASTIC in 1 CARTON (83324-081-60) / 60 TABLET in 1 BOTTLE, PLASTIC2024-04-26NoNoCurrent