Product NDC: | 64141-010 |
Proprietary Name: | TINTED MOISTURIZER |
Non Proprietary Name: | OCTINOXATE, TITANIUM DIOXIDE |
Active Ingredient(s): | 3.5; 1.8 mL/100mL; mL/100mL & nbsp; OCTINOXATE, TITANIUM DIOXIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 64141-010 |
Labeler Name: | Bobbi Brown Professional Cosmetics Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20101201 |
Package NDC: | 64141-010-01 |
Package Description: | 1 TUBE in 1 CARTON (64141-010-01) > 50 mL in 1 TUBE (64141-010-02) |
NDC Code | 64141-010-01 |
Proprietary Name | TINTED MOISTURIZER |
Package Description | 1 TUBE in 1 CARTON (64141-010-01) > 50 mL in 1 TUBE (64141-010-02) |
Product NDC | 64141-010 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE, TITANIUM DIOXIDE |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20101201 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Bobbi Brown Professional Cosmetics Inc. |
Substance Name | OCTINOXATE; TITANIUM DIOXIDE |
Strength Number | 3.5; 1.8 |
Strength Unit | mL/100mL; mL/100mL |
Pharmaceutical Classes |