| 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 |