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