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ULTRA CORRECTION LIFT - 68745-1081-1 - (AVOBENZONE and OCTINOXATE)

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Drug Information of ULTRA CORRECTION LIFT

Product NDC: 68745-1081
Proprietary Name: ULTRA CORRECTION LIFT
Non Proprietary Name: AVOBENZONE and OCTINOXATE
Active Ingredient(s): 1.5; 3.75    mL/50mL; mL/50mL & nbsp;   AVOBENZONE and OCTINOXATE
Administration Route(s): TOPICAL
Dosage Form(s): EMULSION
Coding System: National Drug Codes(NDC)

Labeler Information of ULTRA CORRECTION LIFT

Product NDC: 68745-1081
Labeler Name: CHANEL PARFUMS BEAUTE
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20120801

Package Information of ULTRA CORRECTION LIFT

Package NDC: 68745-1081-1
Package Description: 1 BOTTLE, PUMP in 1 CARTON (68745-1081-1) > 50 mL in 1 BOTTLE, PUMP

NDC Information of ULTRA CORRECTION LIFT

NDC Code 68745-1081-1
Proprietary Name ULTRA CORRECTION LIFT
Package Description 1 BOTTLE, PUMP in 1 CARTON (68745-1081-1) > 50 mL in 1 BOTTLE, PUMP
Product NDC 68745-1081
Product Type Name HUMAN OTC DRUG
Non Proprietary Name AVOBENZONE and OCTINOXATE
Dosage Form Name EMULSION
Route Name TOPICAL
Start Marketing Date 20120801
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name CHANEL PARFUMS BEAUTE
Substance Name AVOBENZONE; OCTINOXATE
Strength Number 1.5; 3.75
Strength Unit mL/50mL; mL/50mL
Pharmaceutical Classes

Complete Information of ULTRA CORRECTION LIFT


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