Uline Acetaminophen Extra Strength

Product NDC
69790-154
11-digit product format
697900154
Labeler code
69790
Product ID
69790-154_3e5d8ade-be5f-4cfa-e063-6394a90a99f6
Type
HUMAN OTC DRUG
Nonproprietary name
acetaminophen
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Uline
Application
M013
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2024-01-30
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
Uline Acetaminophen 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
90167594-0a49-2492-e053-2a95a90a1401Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69790-154-33Uline Acetaminophen Extra Strength2 in 1 PACKETTABLET, FILM COATED28
69790-154-33Uline Acetaminophen Extra Strength50 in 1 BOXTABLET, FILM COATED508

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69790-154ULINE ACETAMINOPHEN EXTRA STRENGTH (ACETAMINOPHEN) TABLET, FILM COATED [ULINE]7Current NDC, 2 package rows20240131_90167594-0a49-2492-e053-2a95a90a1401.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 59 of 79 · 1,579 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Pain Relief Regular StrengthACETAMINOPHENMARC GLASSMAN, INC.e21e821c-9694-5db0-e053-2995a90ad0342024-10-22WarningsExact identifier
application number: M013
Pain Relief Extra StrengthACETAMINOPHENMARC GLASSMAN, INC.e21e90e8-b9f1-1133-e053-2995a90a664b2024-10-22WarningsExact identifier
application number: M013
aspirinASPIRINPublix Super Markets Incc51dae48-aa49-4926-b04a-0da264e08dfa2024-10-22WarningsExact identifier
application number: M013
Acetaminophen Extra StrengthACETAMINOPHENKROGER COMPANYb96a2280-ec4f-7c61-e053-2995a90a18bb2024-10-22WarningsExact identifier
application number: M013
Pain Relief Extra StrengthACETAMINOPHENHEBf17a18b0-a7c2-4c64-868c-460cf34e1f7d2024-10-21WarningsExact identifier
application number: M013
Pain Relief Extra StrengthACETAMINOPHENHEB0863aeaa-15ec-4c67-ba79-4dad54555bd22024-10-21WarningsExact identifier
application number: M013
AcetaminophenACETAMINOPHENAmerican Health Packaging3c0175a0-175b-48b8-9192-3f869690c0f22024-10-21WarningsExact identifier
application number: M013
AcetaminophenACETAMINOPHENAmerican Health Packaging0d6553bd-3e18-4624-a83a-899bcafb32722024-10-21WarningsExact identifier
application number: M013
Childrens Acetaminophen Oral SuspensionACETAMINOPHENAmerican Health Packaging8231dd91-e9e6-4350-a485-fa95d65a6d252024-10-21WarningsExact identifier
application number: M013
Acetaminophen Extra StrengthACETAMINOPHENKROGER COMPANYcf63c372-acdd-6e6e-e053-2995a90a16622024-10-21WarningsExact identifier
application number: M013
good sense pain reliefACETAMINOPHENL. Perrigo Company8b56bfc0-2253-458d-99a6-0b0f9ae0ba502024-10-21WarningsExact identifier
application number: M013
AspirinASPIRINGOODSENSE662a2bc6-9507-465c-b467-7ae1b2e1dedc2024-10-18WarningsExact identifier
application number: M013
Pain Relief Extra StrengthACETAMINOPHENGoodSenseda4339c0-1822-41d8-8c20-214c379a5aa72024-10-18WarningsExact identifier
application number: M013
Pain Relief PM Extra StrengthACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDEGoodSense8972d95a-51da-40b5-8ef1-9dfed220d7eb2024-10-18WarningsExact identifier
application number: M013
Pain Relief Regular StrengthACETAMINOPHENAmeriSource Bergend571f520-a56e-4f7f-9214-d89197f742b62024-10-18WarningsExact identifier
application number: M013
LOW DOSE ASPIRINASPIRINBryant Ranch Prepack6b4b7f72-dac8-4b59-a58c-7c59d4b1ef322024-10-18WarningsExact identifier
application number: M013
dg health pain reliefACETAMINOPHENDolgencorp Inc2e1470f5-e88f-4d1d-a308-170f7080387e2024-10-17WarningsExact identifier
application number: M013
Pain ReliefACETAMINOPHENDISCOUNT DRUG MART146c735b-5081-4de4-9025-d939d560bbba2024-10-17WarningsExact identifier
application number: M013
Chewable AspirinASPIRINDISCOUNT DRUG MARTc8483d64-874c-3056-e053-2995a90ad8aa2024-10-17WarningsExact identifier
application number: M013
Adult Chewable AspirinASPIRINDISCOUNT DRUG MARTc8484998-e0e1-ffce-e053-2995a90aa7de2024-10-17WarningsExact identifier
application number: M013

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
198440acetaminophen 500 MG Oral TabletPSN90167594-0a49-2492-e053-2a95a90a14018
198440acetaminophen 500 MG Oral TabletSCD90167594-0a49-2492-e053-2a95a90a14018
198440APAP 500 MG Oral TabletSY90167594-0a49-2492-e053-2a95a90a14018

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
69790-154-336979001543350 PACKET in 1 BOX (69790-154-33) / 2 TABLET, FILM COATED in 1 PACKET50 packet2024-01-30NoNoCurrent