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Resilience Lift Extreme - 11559-967-01 - (OCTINOXATE and TITANIUM DIOXIDE)

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Drug Information of Resilience Lift Extreme

Product NDC: 11559-967
Proprietary Name: Resilience Lift Extreme
Non Proprietary Name: OCTINOXATE and TITANIUM DIOXIDE
Active Ingredient(s): 4.2; 1    mL/100mL; mL/100mL & nbsp;   OCTINOXATE and TITANIUM DIOXIDE
Administration Route(s): TOPICAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Resilience Lift Extreme

Product NDC: 11559-967
Labeler Name: Estee Lauder Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20060601

Package Information of Resilience Lift Extreme

Package NDC: 11559-967-01
Package Description: 1 BOTTLE in 1 CARTON (11559-967-01) > 30 mL in 1 BOTTLE

NDC Information of Resilience Lift Extreme

NDC Code 11559-967-01
Proprietary Name Resilience Lift Extreme
Package Description 1 BOTTLE in 1 CARTON (11559-967-01) > 30 mL in 1 BOTTLE
Product NDC 11559-967
Product Type Name HUMAN OTC DRUG
Non Proprietary Name OCTINOXATE and TITANIUM DIOXIDE
Dosage Form Name LIQUID
Route Name TOPICAL
Start Marketing Date 20060601
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Estee Lauder Inc.
Substance Name OCTINOXATE; TITANIUM DIOXIDE
Strength Number 4.2; 1
Strength Unit mL/100mL; mL/100mL
Pharmaceutical Classes

Complete Information of Resilience Lift Extreme


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