Pain Reliever

Product NDC
83059-0103
11-digit product format
830590103
Labeler code
83059
Product ID
83059-0103_43073225-59e2-7d5d-e063-6394a90a17d8
Type
HUMAN OTC DRUG
Nonproprietary name
Acetaminophen
Dosage form
TABLET
Route
ORAL
Labeler
Shield Pharmaceuticals Corp
Application
M013
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-11-07
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 Reliever
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
83059-0103-5Pain Reliever50 in 1 BOTTLETABLET502

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
198440acetaminophen 500 MG Oral TabletPSN61e50135-a7c2-4a86-8a1a-d47b41d3f9d12
198440acetaminophen 500 MG Oral TabletSCD61e50135-a7c2-4a86-8a1a-d47b41d3f9d12
198440APAP 500 MG Oral TabletSY61e50135-a7c2-4a86-8a1a-d47b41d3f9d12

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
83059-0103-58305901030550 TABLET in 1 BOTTLE (83059-0103-5) 50 tablet2025-11-07NoNoCurrent