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UV ESSENTIEL - 68745-1150-2 - (Multi-Protection Daily UV Care)

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Drug Information of UV ESSENTIEL

Product NDC: 68745-1150
Proprietary Name: UV ESSENTIEL
Non Proprietary Name: Multi-Protection Daily UV Care
Active Ingredient(s): 2.25; .6; 5.13    mL/30mL; mL/30mL; mL/30mL & nbsp;   Multi-Protection Daily UV Care
Administration Route(s): TOPICAL
Dosage Form(s): EMULSION
Coding System: National Drug Codes(NDC)

Labeler Information of UV ESSENTIEL

Product NDC: 68745-1150
Labeler Name: CHANEL PARFUMS BEAUTE
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20100301

Package Information of UV ESSENTIEL

Package NDC: 68745-1150-2
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (68745-1150-2) > 30 mL in 1 BOTTLE, PLASTIC (68745-1150-1)

NDC Information of UV ESSENTIEL

NDC Code 68745-1150-2
Proprietary Name UV ESSENTIEL
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (68745-1150-2) > 30 mL in 1 BOTTLE, PLASTIC (68745-1150-1)
Product NDC 68745-1150
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Multi-Protection Daily UV Care
Dosage Form Name EMULSION
Route Name TOPICAL
Start Marketing Date 20100301
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name CHANEL PARFUMS BEAUTE
Substance Name OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE
Strength Number 2.25; .6; 5.13
Strength Unit mL/30mL; mL/30mL; mL/30mL
Pharmaceutical Classes

Complete Information of UV ESSENTIEL


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