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BOBBI BROWN SKIN FOUNDATION
BOBBI BROWN SKIN FOUNDATION - 64141-001-01 - (OCTINOXATE 7.5, TITANIUM DIOXIDE 1.0%)
Drug Information of BOBBI BROWN SKIN FOUNDATION
| Product NDC: | 64141-001 |
| Proprietary Name: | BOBBI BROWN SKIN FOUNDATION |
| Non Proprietary Name: | OCTINOXATE 7.5, TITANIUM DIOXIDE 1.0% |
| Active Ingredient(s): | 7.5; 1 mL/100mL; mL/100mL & nbsp; OCTINOXATE 7.5, TITANIUM DIOXIDE 1.0% |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of BOBBI BROWN SKIN FOUNDATION
| Product NDC: | 64141-001 |
| 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: | 20080601 |
Package Information of BOBBI BROWN SKIN FOUNDATION
| Package NDC: | 64141-001-01 |
| Package Description: | 1 BOTTLE, GLASS in 1 CARTON (64141-001-01) > 30 mL in 1 BOTTLE, GLASS (64141-001-02) |
NDC Information of BOBBI BROWN SKIN FOUNDATION
| NDC Code | 64141-001-01 |
| Proprietary Name | BOBBI BROWN SKIN FOUNDATION |
| Package Description | 1 BOTTLE, GLASS in 1 CARTON (64141-001-01) > 30 mL in 1 BOTTLE, GLASS (64141-001-02) |
| Product NDC | 64141-001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE 7.5, TITANIUM DIOXIDE 1.0% |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20080601 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | BOBBI BROWN PROFESSIONAL COSMETICS INC |
| Substance Name | OCTINOXATE; TITANIUM DIOXIDE |
| Strength Number | 7.5; 1 |
| Strength Unit | mL/100mL; mL/100mL |
| Pharmaceutical Classes |
