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Sunscreen Baby - 29565-300-50 - (Zinc oxide)

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Drug Information of Sunscreen Baby

Product NDC: 29565-300
Proprietary Name: Sunscreen Baby
Non Proprietary Name: Zinc oxide
Active Ingredient(s): 12.9    mL/52mL & nbsp;   Zinc oxide
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of Sunscreen Baby

Product NDC: 29565-300
Labeler Name: UV Natural International Pty Ltd
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20060101

Package Information of Sunscreen Baby

Package NDC: 29565-300-50
Package Description: 156 mL in 1 TUBE (29565-300-50)

NDC Information of Sunscreen Baby

NDC Code 29565-300-50
Proprietary Name Sunscreen Baby
Package Description 156 mL in 1 TUBE (29565-300-50)
Product NDC 29565-300
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Zinc oxide
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20060101
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name UV Natural International Pty Ltd
Substance Name ZINC OXIDE
Strength Number 12.9
Strength Unit mL/52mL
Pharmaceutical Classes

Complete Information of Sunscreen Baby


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