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Ultra Seal Bacitracin - 42213-400-28 - (BACITRACIN ZINC)

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Drug Information of Ultra Seal Bacitracin

Product NDC: 42213-400
Proprietary Name: Ultra Seal Bacitracin
Non Proprietary Name: BACITRACIN ZINC
Active Ingredient(s): 500    [iU]/g & nbsp;   BACITRACIN ZINC
Administration Route(s): TOPICAL
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of Ultra Seal Bacitracin

Product NDC: 42213-400
Labeler Name: Ultra Seal Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: part333B
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20111204

Package Information of Ultra Seal Bacitracin

Package NDC: 42213-400-28
Package Description: 1 TUBE in 1 CARTON (42213-400-28) > 28 g in 1 TUBE

NDC Information of Ultra Seal Bacitracin

NDC Code 42213-400-28
Proprietary Name Ultra Seal Bacitracin
Package Description 1 TUBE in 1 CARTON (42213-400-28) > 28 g in 1 TUBE
Product NDC 42213-400
Product Type Name HUMAN OTC DRUG
Non Proprietary Name BACITRACIN ZINC
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 20111204
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Ultra Seal Corporation
Substance Name BACITRACIN ZINC
Strength Number 500
Strength Unit [iU]/g
Pharmaceutical Classes

Complete Information of Ultra Seal Bacitracin


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