NDC 58232-4033

Polysporin

Polymyxin B Sulfate And Bacitracin Zinc

Polysporin is a Topical Powder in the Human Otc Drug category. It is labeled and distributed by Johnson & Johnson Consumer Products Company, Division Of Johnson & Johnson Consumer Companies, Inc.. The primary component is Polymyxin B Sulfate; Bacitracin Zinc.

Product ID58232-4033_20f2bbe4-38a2-48f5-a211-abbc2c9176fa
NDC58232-4033
Product TypeHuman Otc Drug
Proprietary NamePolysporin
Generic NamePolymyxin B Sulfate And Bacitracin Zinc
Dosage FormPowder
Route of AdministrationTOPICAL
Marketing Start Date2010-06-14
Marketing CategoryOTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
Application Numberpart333
Labeler NameJohnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc.
Substance NamePOLYMYXIN B SULFATE; BACITRACIN ZINC
Active Ingredient Strength10000 [USP'U]/g; [USP'U]/g
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 58232-4033-1

1 BOTTLE in 1 CARTON (58232-4033-1) > 10 g in 1 BOTTLE
Marketing Start Date2010-06-14
Marketing End Date2023-12-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 58232-4033-1 [58232403301]

Polysporin POWDER
Marketing CategoryOTC MONOGRAPH FINAL
Application Numberpart333B
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-06-14
Marketing End Date2023-12-01

Drug Details

Active Ingredients

IngredientStrength
POLYMYXIN B SULFATE10000 [USP'U]/g

OpenFDA Data

SPL SET ID:0b0c5a93-4a2a-45dc-9800-55c914369b63
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 308513
  • 212240

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