Sunscreen - 29565-200-10 - (Zinc oxide)

Alphabetical Index


Drug Information of Sunscreen

Product NDC: 29565-200
Proprietary Name: Sunscreen
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

Product NDC: 29565-200
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

Package NDC: 29565-200-10
Package Description: 52 mL in 1 TUBE (29565-200-10)

NDC Information of Sunscreen

NDC Code 29565-200-10
Proprietary Name Sunscreen
Package Description 52 mL in 1 TUBE (29565-200-10)
Product NDC 29565-200
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


General Information