Product NDC: | 64141-113 |
Proprietary Name: | BOBBIE BROWN CORRECTIVE SPOT TREATMENT BROAD SPECTRUM |
Non Proprietary Name: | OCTINOXATE and TITANIUM DIOXIDE |
Active Ingredient(s): | 98; 15.4 mg/mL; mg/mL & nbsp; OCTINOXATE and TITANIUM DIOXIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 64141-113 |
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: | 20120410 |
Package NDC: | 64141-113-01 |
Package Description: | 1 TUBE in 1 CARTON (64141-113-01) > 4.5 mL in 1 TUBE |
NDC Code | 64141-113-01 |
Proprietary Name | BOBBIE BROWN CORRECTIVE SPOT TREATMENT BROAD SPECTRUM |
Package Description | 1 TUBE in 1 CARTON (64141-113-01) > 4.5 mL in 1 TUBE |
Product NDC | 64141-113 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE and TITANIUM DIOXIDE |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20120410 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Bobbi Brown Professional Cosmetics Inc. |
Substance Name | OCTINOXATE; TITANIUM DIOXIDE |
Strength Number | 98; 15.4 |
Strength Unit | mg/mL; mg/mL |
Pharmaceutical Classes |