Product NDC: | 64141-005 |
Proprietary Name: | BOBBI BROWN BRIGHTENING PROTECTIVE FACE BASE |
Non Proprietary Name: | HOMOSALATE, OCTISALATE, AVOBENZONE, OXYBENZONE |
Active Ingredient(s): | 3; 5; 5; 3 mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp; HOMOSALATE, OCTISALATE, AVOBENZONE, OXYBENZONE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 64141-005 |
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: | 20100713 |
Package NDC: | 64141-005-01 |
Package Description: | 1 TUBE in 1 CARTON (64141-005-01) > 50 mL in 1 TUBE (64141-005-02) |
NDC Code | 64141-005-01 |
Proprietary Name | BOBBI BROWN BRIGHTENING PROTECTIVE FACE BASE |
Package Description | 1 TUBE in 1 CARTON (64141-005-01) > 50 mL in 1 TUBE (64141-005-02) |
Product NDC | 64141-005 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | HOMOSALATE, OCTISALATE, AVOBENZONE, OXYBENZONE |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20100713 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Bobbi Brown Professional Cosmetics Inc. |
Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OXYBENZONE |
Strength Number | 3; 5; 5; 3 |
Strength Unit | mL/100mL; mL/100mL; mL/100mL; mL/100mL |
Pharmaceutical Classes |