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BOBBI BROWN BB
BOBBI BROWN BB - 64141-012-01 - (OCTINOXATE, OCTISALATE, OXYBENZONE, and TITANIUM DIOXIDE)
Drug Information of BOBBI BROWN BB
| Product NDC: | 64141-012 |
| Proprietary Name: | BOBBI BROWN BB |
| Non Proprietary Name: | OCTINOXATE, OCTISALATE, OXYBENZONE, and TITANIUM DIOXIDE |
| Active Ingredient(s): | 7.5; 4; 2.5; 1.1 mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp; OCTINOXATE, OCTISALATE, OXYBENZONE, and TITANIUM DIOXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of BOBBI BROWN BB
| Product NDC: | 64141-012 |
| 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: | 20101201 |
Package Information of BOBBI BROWN BB
| Package NDC: | 64141-012-01 |
| Package Description: | 1 BOTTLE in 1 CARTON (64141-012-01) > 40 mL in 1 BOTTLE |
NDC Information of BOBBI BROWN BB
| NDC Code | 64141-012-01 |
| Proprietary Name | BOBBI BROWN BB |
| Package Description | 1 BOTTLE in 1 CARTON (64141-012-01) > 40 mL in 1 BOTTLE |
| Product NDC | 64141-012 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, OCTISALATE, OXYBENZONE, and TITANIUM DIOXIDE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20101201 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Bobbi Brown Professional Cosmetics Inc. |
| Substance Name | OCTINOXATE; OCTISALATE; OXYBENZONE; TITANIUM DIOXIDE |
| Strength Number | 7.5; 4; 2.5; 1.1 |
| Strength Unit | mL/100mL; mL/100mL; mL/100mL; mL/100mL |
| Pharmaceutical Classes |
