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BRIGHTENING POWDER
BRIGHTENING POWDER - 64141-718-01 - (TITANIUM DIOXIDE, OCTINOXATE, ZINC OXIDE)
Drug Information of BRIGHTENING POWDER
| Product NDC: | 64141-718 |
| Proprietary Name: | BRIGHTENING POWDER |
| Non Proprietary Name: | TITANIUM DIOXIDE, OCTINOXATE, ZINC OXIDE |
| Active Ingredient(s): | 7; 18.6; 5.8 g/100g; g/100g; g/100g & nbsp; TITANIUM DIOXIDE, OCTINOXATE, ZINC OXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | POWDER |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of BRIGHTENING POWDER
| Product NDC: | 64141-718 |
| 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: | 20050901 |
Package Information of BRIGHTENING POWDER
| Package NDC: | 64141-718-01 |
| Package Description: | 1 JAR in 1 CARTON (64141-718-01) > 11 g in 1 JAR (64141-718-02) |
NDC Information of BRIGHTENING POWDER
| NDC Code | 64141-718-01 |
| Proprietary Name | BRIGHTENING POWDER |
| Package Description | 1 JAR in 1 CARTON (64141-718-01) > 11 g in 1 JAR (64141-718-02) |
| Product NDC | 64141-718 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | TITANIUM DIOXIDE, OCTINOXATE, ZINC OXIDE |
| Dosage Form Name | POWDER |
| Route Name | TOPICAL |
| Start Marketing Date | 20050901 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Bobbi Brown Professional Cosmetics Inc. |
| Substance Name | OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | 7; 18.6; 5.8 |
| Strength Unit | g/100g; g/100g; g/100g |
| Pharmaceutical Classes |
