Home
>
National Drug Code (NDC)
>
BOBBI BROWN SKIN FOUNDATION
BOBBI BROWN SKIN FOUNDATION - 64141-013-01 - (OCTINOXATE and TITANIUM DIOXIDE)
Drug Information of BOBBI BROWN SKIN FOUNDATION
| Product NDC: | 64141-013 |
| Proprietary Name: | BOBBI BROWN SKIN FOUNDATION |
| Non Proprietary Name: | OCTINOXATE and TITANIUM DIOXIDE |
| Active Ingredient(s): | .078; .0104 g/mL; g/mL & nbsp; OCTINOXATE and TITANIUM DIOXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of BOBBI BROWN SKIN FOUNDATION
| Product NDC: | 64141-013 |
| 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: | 20120901 |
Package Information of BOBBI BROWN SKIN FOUNDATION
| Package NDC: | 64141-013-01 |
| Package Description: | 1 BOTTLE in 1 CARTON (64141-013-01) > 30 mL in 1 BOTTLE |
NDC Information of BOBBI BROWN SKIN FOUNDATION
| NDC Code | 64141-013-01 |
| Proprietary Name | BOBBI BROWN SKIN FOUNDATION |
| Package Description | 1 BOTTLE in 1 CARTON (64141-013-01) > 30 mL in 1 BOTTLE |
| Product NDC | 64141-013 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE and TITANIUM DIOXIDE |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20120901 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Bobbi Brown Professional Cosmetics Inc. |
| Substance Name | OCTINOXATE; TITANIUM DIOXIDE |
| Strength Number | .078; .0104 |
| Strength Unit | g/mL; g/mL |
| Pharmaceutical Classes |
