Zinc Oxide - 42213-365-48 - (Zinc Oxide)

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Drug Information of Zinc Oxide

Product NDC: 42213-365
Proprietary Name: Zinc Oxide
Non Proprietary Name: Zinc Oxide
Active Ingredient(s): 200    mg/g & nbsp;   Zinc Oxide
Administration Route(s): TOPICAL
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of Zinc Oxide

Product NDC: 42213-365
Labeler Name: Ultra Seal Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: part347
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20120503

Package Information of Zinc Oxide

Package NDC: 42213-365-48
Package Description: 1 TUBE in 1 CARTON (42213-365-48) > 56 g in 1 TUBE (42213-365-56)

NDC Information of Zinc Oxide

NDC Code 42213-365-48
Proprietary Name Zinc Oxide
Package Description 1 TUBE in 1 CARTON (42213-365-48) > 56 g in 1 TUBE (42213-365-56)
Product NDC 42213-365
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Zinc Oxide
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 20120503
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Ultra Seal Corporation
Substance Name ZINC OXIDE
Strength Number 200
Strength Unit mg/g
Pharmaceutical Classes

Complete Information of Zinc Oxide


General Information