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