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bronze-n-brighten
bronze-n-brighten - 51389-105-01 - (TITANIUM DIOXIDE)
Drug Information of bronze-n-brighten
| Product NDC: | 51389-105 |
| Proprietary Name: | bronze-n-brighten |
| Non Proprietary Name: | TITANIUM DIOXIDE |
| Active Ingredient(s): | 10 g/100g & nbsp; TITANIUM DIOXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | POWDER |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of bronze-n-brighten
| Product NDC: | 51389-105 |
| Labeler Name: | LAURA GELLER MAKE UP INC. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20111113 |
Package Information of bronze-n-brighten
| Package NDC: | 51389-105-01 |
| Package Description: | 1 CONTAINER in 1 KIT (51389-105-01) > 9 g in 1 CONTAINER |
NDC Information of bronze-n-brighten
| NDC Code | 51389-105-01 |
| Proprietary Name | bronze-n-brighten |
| Package Description | 1 CONTAINER in 1 KIT (51389-105-01) > 9 g in 1 CONTAINER |
| Product NDC | 51389-105 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | TITANIUM DIOXIDE |
| Dosage Form Name | POWDER |
| Route Name | TOPICAL |
| Start Marketing Date | 20111113 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | LAURA GELLER MAKE UP INC. |
| Substance Name | TITANIUM DIOXIDE |
| Strength Number | 10 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
