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PROVENCE FOUNDATION - 51346-202-01 - (Titanium Dioxide, OCTINOXATE, Zinc Oxide)

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Drug Information of PROVENCE FOUNDATION

Product NDC: 51346-202
Proprietary Name: PROVENCE FOUNDATION
Non Proprietary Name: Titanium Dioxide, OCTINOXATE, Zinc Oxide
Active Ingredient(s): 1.4; 3.65; .34    mg/35mL; mg/35mL; mg/35mL & nbsp;   Titanium Dioxide, OCTINOXATE, Zinc Oxide
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of PROVENCE FOUNDATION

Product NDC: 51346-202
Labeler Name: NATURE REPUBLIC CO., LTD.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20130201

Package Information of PROVENCE FOUNDATION

Package NDC: 51346-202-01
Package Description: 35 mL in 1 CARTON (51346-202-01)

NDC Information of PROVENCE FOUNDATION

NDC Code 51346-202-01
Proprietary Name PROVENCE FOUNDATION
Package Description 35 mL in 1 CARTON (51346-202-01)
Product NDC 51346-202
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Titanium Dioxide, OCTINOXATE, Zinc Oxide
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20130201
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name NATURE REPUBLIC CO., LTD.
Substance Name OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE
Strength Number 1.4; 3.65; .34
Strength Unit mg/35mL; mg/35mL; mg/35mL
Pharmaceutical Classes

Complete Information of PROVENCE FOUNDATION


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