Product NDC: | 11559-746 |
Proprietary Name: | RENUTRIV |
Non Proprietary Name: | OCTINOXATE, TITANIUM DIOXIDE |
Active Ingredient(s): | 2.2; 1.4 mL/100mL; mL/100mL & nbsp; OCTINOXATE, TITANIUM DIOXIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 11559-746 |
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: | 11559-746-01 |
Package Description: | 1 BOTTLE in 1 CARTON (11559-746-01) > 30 mL in 1 BOTTLE (11559-746-02) |
NDC Code | 11559-746-01 |
Proprietary Name | RENUTRIV |
Package Description | 1 BOTTLE in 1 CARTON (11559-746-01) > 30 mL in 1 BOTTLE (11559-746-02) |
Product NDC | 11559-746 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE, TITANIUM DIOXIDE |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20100901 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | ESTEE LAUDER INC |
Substance Name | OCTINOXATE; TITANIUM DIOXIDE |
Strength Number | 2.2; 1.4 |
Strength Unit | mL/100mL; mL/100mL |
Pharmaceutical Classes |