| Product NDC: | 64141-007 |
| Proprietary Name: | ILLUMINATING FINISH |
| Non Proprietary Name: | TITANIUM DIOXIDE, OCTINOXATE |
| Active Ingredient(s): | 3; 6.3 g/100g; g/100g & nbsp; TITANIUM DIOXIDE, OCTINOXATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | POWDER |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 64141-007 |
| 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: | 20100701 |
| Package NDC: | 64141-007-01 |
| Package Description: | 1 CASE in 1 CARTON (64141-007-01) > 13 g in 1 CASE (64141-007-02) |
| NDC Code | 64141-007-01 |
| Proprietary Name | ILLUMINATING FINISH |
| Package Description | 1 CASE in 1 CARTON (64141-007-01) > 13 g in 1 CASE (64141-007-02) |
| Product NDC | 64141-007 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | TITANIUM DIOXIDE, OCTINOXATE |
| Dosage Form Name | POWDER |
| Route Name | TOPICAL |
| Start Marketing Date | 20100701 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Bobbi Brown Professional Cosmetics Inc. |
| Substance Name | OCTINOXATE; TITANIUM DIOXIDE |
| Strength Number | 3; 6.3 |
| Strength Unit | g/100g; g/100g |
| Pharmaceutical Classes |