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BOBBI BROWN PROTECTIVE FACE
BOBBI BROWN PROTECTIVE FACE - 64141-866-01 - (OCTINOXATE, TITANIUM DIOXIDE)
Drug Information of BOBBI BROWN PROTECTIVE FACE
| Product NDC: | 64141-866 |
| Proprietary Name: | BOBBI BROWN PROTECTIVE FACE |
| Non Proprietary Name: | OCTINOXATE, TITANIUM DIOXIDE |
| Active Ingredient(s): | 7.5; 1.2 mL/100mL; mL/100mL & nbsp; OCTINOXATE, TITANIUM DIOXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of BOBBI BROWN PROTECTIVE FACE
| Product NDC: | 64141-866 |
| 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: | 20100706 |
Package Information of BOBBI BROWN PROTECTIVE FACE
| Package NDC: | 64141-866-01 |
| Package Description: | 1 BOTTLE in 1 CARTON (64141-866-01) > 50 mL in 1 BOTTLE (64141-866-02) |
NDC Information of BOBBI BROWN PROTECTIVE FACE
| NDC Code | 64141-866-01 |
| Proprietary Name | BOBBI BROWN PROTECTIVE FACE |
| Package Description | 1 BOTTLE in 1 CARTON (64141-866-01) > 50 mL in 1 BOTTLE (64141-866-02) |
| Product NDC | 64141-866 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, TITANIUM DIOXIDE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20100706 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Bobbi Brown Professional Cosmetics Inc. |
| Substance Name | OCTINOXATE; TITANIUM DIOXIDE |
| Strength Number | 7.5; 1.2 |
| Strength Unit | mL/100mL; mL/100mL |
| Pharmaceutical Classes |
