NDC 51852-100

First Aid Triple Antibiotic and Pain Relief Maximum Strength

Bacitracin Zinc, Neomycin, Polymyxin B Sulfate, Pramoxine Hydrocloride

First Aid Triple Antibiotic and Pain Relief Maximum Strength is a Topical Ointment in the Human Otc Drug category. It is labeled and distributed by Lifelabs, A Division Of Atico International Usa, Inc.. The primary component is Bacitracin Zinc; Neomycin Sulfate; Polymyxin B Sulfate; Pramoxine Hydrochloride.

Product ID51852-100_cf361d71-0209-4d1d-af56-c29648c5d3fd
NDC51852-100
Product TypeHuman Otc Drug
Proprietary NameFirst Aid Triple Antibiotic and Pain Relief Maximum Strength
Generic NameBacitracin Zinc, Neomycin, Polymyxin B Sulfate, Pramoxine Hydrocloride
Dosage FormOintment
Route of AdministrationTOPICAL
Marketing Start Date2010-11-01
Marketing CategoryOTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
Application Numberpart333B
Labeler NameLIFElabs, a Division of Atico International USA, INC.
Substance NameBACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE; PRAMOXINE HYDROCHLORIDE
Active Ingredient Strength500 [USP'U]/g; mg/g; [USP'U]/g; mg/g
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 51852-100-01

1 TUBE in 1 CARTON (51852-100-01) > 28 g in 1 TUBE
Marketing Start Date2010-11-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 51852-100-01 [51852010001]

First Aid Triple Antibiotic and Pain Relief Maximum Strength OINTMENT
Marketing CategoryOTC monograph final
Application Numberpart333B
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-11-01
Inactivation Date2019-10-29

Drug Details

Active Ingredients

IngredientStrength
BACITRACIN ZINC500 [USP'U]/g

OpenFDA Data

SPL SET ID:db368653-fce9-4773-af14-08067409529f
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1359350
  • UPC Code
  • 0000000000000

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