NDC 49580-0281

Pain Reliever Childrens

Acetaminophen

Pain Reliever Childrens is a Oral Suspension in the Human Otc Drug category. It is labeled and distributed by P & L Development, Llc. The primary component is Acetaminophen.

Product ID49580-0281_7ff6ef83-c549-488c-9faa-30bfcc1dc311
NDC49580-0281
Product TypeHuman Otc Drug
Proprietary NamePain Reliever Childrens
Generic NameAcetaminophen
Dosage FormSuspension
Route of AdministrationORAL
Marketing Start Date2016-04-30
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart343
Labeler NameP & L Development, LLC
Substance NameACETAMINOPHEN
Active Ingredient Strength160 mg/5mL
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 49580-0281-4

1 BOTTLE in 1 BOX (49580-0281-4) > 118 mL in 1 BOTTLE
Marketing Start Date2016-04-30
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 49580-0281-4 [49580028104]

Pain Reliever Childrens SUSPENSION
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-04-30

Drug Details

Active Ingredients

IngredientStrength
ACETAMINOPHEN160 mg/5mL

OpenFDA Data

SPL SET ID:f5ad8344-72a9-40a0-8fbc-a6c1699d9769
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 307668
  • UPC Code
  • 0349580281042