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BRIGHTENING SPOT TREATMENT CORRECTOR
BRIGHTENING SPOT TREATMENT CORRECTOR - 64141-003-01 - (OCTINOXATE, TITANIUM DIOXIDE)
Drug Information of BRIGHTENING SPOT TREATMENT CORRECTOR
| Product NDC: | 64141-003 |
| Proprietary Name: | BRIGHTENING SPOT TREATMENT CORRECTOR |
| Non Proprietary Name: | OCTINOXATE, TITANIUM DIOXIDE |
| Active Ingredient(s): | 7; .98 mL/100mL; mL/100mL & nbsp; OCTINOXATE, TITANIUM DIOXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of BRIGHTENING SPOT TREATMENT CORRECTOR
| Product NDC: | 64141-003 |
| 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: | 20090301 |
Package Information of BRIGHTENING SPOT TREATMENT CORRECTOR
| Package NDC: | 64141-003-01 |
| Package Description: | 1 TUBE, WITH APPLICATOR in 1 CARTON (64141-003-01) > 4.5 mL in 1 TUBE, WITH APPLICATOR (64141-003-02) |
NDC Information of BRIGHTENING SPOT TREATMENT CORRECTOR
| NDC Code | 64141-003-01 |
| Proprietary Name | BRIGHTENING SPOT TREATMENT CORRECTOR |
| Package Description | 1 TUBE, WITH APPLICATOR in 1 CARTON (64141-003-01) > 4.5 mL in 1 TUBE, WITH APPLICATOR (64141-003-02) |
| Product NDC | 64141-003 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, TITANIUM DIOXIDE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20090301 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Bobbi Brown Professional Cosmetics Inc |
| Substance Name | OCTINOXATE; TITANIUM DIOXIDE |
| Strength Number | 7; .98 |
| Strength Unit | mL/100mL; mL/100mL |
| Pharmaceutical Classes |
