Pain Relief

Product NDC
55910-135
11-digit product format
559100135
Labeler code
55910
Product ID
55910-135_2a0bb74a-3945-4bd9-b9ab-1331884fee78
Type
HUMAN OTC DRUG
Nonproprietary name
Acetaminophen
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
DOLGENCORP, LLC
Application
M013
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2024-06-07
Substance
ACETAMINOPHEN
Active strength
500 mg/1
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
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ACETAMINOPHEN500 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii362O9ITL9D
Rxcui198440

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55910-135-15Pain Relief50 in 1 BOTTLE, PLASTICTABLET, FILM COATED503
55910-135-15Pain Relief1 in 1 BOXTABLET, FILM COATED13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55910-135PAIN RELIEF (ACETAMINOPHEN) TABLET, FILM COATED [DOLGENCORP, LLC]1Current NDC, 2 package rows20240608_acc94a3e-21b6-4375-9881-38cf9bab8692.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
198440acetaminophen 500 MG Oral TabletPSNacc94a3e-21b6-4375-9881-38cf9bab86923
198440acetaminophen 500 MG Oral TabletSCDacc94a3e-21b6-4375-9881-38cf9bab86923
198440APAP 500 MG Oral TabletSYacc94a3e-21b6-4375-9881-38cf9bab86923

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
55910-135-15559100135151 BOTTLE, PLASTIC in 1 BOX (55910-135-15) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC2024-06-07NoNoHistorical