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THE FLOWER UV INTENSE PACT - 51523-024-01 - (ZINC OXIDE)

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Drug Information of THE FLOWER UV INTENSE PACT

Product NDC: 51523-024
Proprietary Name: THE FLOWER UV INTENSE PACT
Non Proprietary Name: ZINC OXIDE
Active Ingredient(s): 1.54; 1.65    g/12g; g/12g & nbsp;   ZINC OXIDE
Administration Route(s): CUTANEOUS
Dosage Form(s): POWDER
Coding System: National Drug Codes(NDC)

Labeler Information of THE FLOWER UV INTENSE PACT

Product NDC: 51523-024
Labeler Name: THEFACESHOP CO., LTD.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20070301

Package Information of THE FLOWER UV INTENSE PACT

Package NDC: 51523-024-01
Package Description: 12 g in 1 CARTON (51523-024-01)

NDC Information of THE FLOWER UV INTENSE PACT

NDC Code 51523-024-01
Proprietary Name THE FLOWER UV INTENSE PACT
Package Description 12 g in 1 CARTON (51523-024-01)
Product NDC 51523-024
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ZINC OXIDE
Dosage Form Name POWDER
Route Name CUTANEOUS
Start Marketing Date 20070301
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name THEFACESHOP CO., LTD.
Substance Name TITANIUM DIOXIDE; ZINC OXIDE
Strength Number 1.54; 1.65
Strength Unit g/12g; g/12g
Pharmaceutical Classes

Complete Information of THE FLOWER UV INTENSE PACT


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