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RESILIENCE LIFT - 11559-012-01 - (OCINOXATE)

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Drug Information of RESILIENCE LIFT

Product NDC: 11559-012
Proprietary Name: RESILIENCE LIFT
Non Proprietary Name: OCINOXATE
Active Ingredient(s): 7.5    mL/100mL & nbsp;   OCINOXATE
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of RESILIENCE LIFT

Product NDC: 11559-012
Labeler Name: ESTEE LAUDER INC
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20100901

Package Information of RESILIENCE LIFT

Package NDC: 11559-012-01
Package Description: 1 JAR in 1 CARTON (11559-012-01) > 50 mL in 1 JAR (11559-012-02)

NDC Information of RESILIENCE LIFT

NDC Code 11559-012-01
Proprietary Name RESILIENCE LIFT
Package Description 1 JAR in 1 CARTON (11559-012-01) > 50 mL in 1 JAR (11559-012-02)
Product NDC 11559-012
Product Type Name HUMAN OTC DRUG
Non Proprietary Name OCINOXATE
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20100901
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name ESTEE LAUDER INC
Substance Name OCTINOXATE
Strength Number 7.5
Strength Unit mL/100mL
Pharmaceutical Classes

Complete Information of RESILIENCE LIFT


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