Home
>
National Drug Code (NDC)
>
BRIGHTEN
BRIGHTEN - 54272-201-11 - (ZINC OXIDE OCTINOXATE)
Drug Information of BRIGHTEN
| Product NDC: | 54272-201 |
| Proprietary Name: | BRIGHTEN |
| Non Proprietary Name: | ZINC OXIDE OCTINOXATE |
| Active Ingredient(s): | 6; 15 g/100mL; g/100mL & nbsp; ZINC OXIDE OCTINOXATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of BRIGHTEN
| Product NDC: | 54272-201 |
| Labeler Name: | CEN BEAUTY LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130221 |
Package Information of BRIGHTEN
| Package NDC: | 54272-201-11 |
| Package Description: | 30 mL in 1 TUBE (54272-201-11) |
NDC Information of BRIGHTEN
| NDC Code | 54272-201-11 |
| Proprietary Name | BRIGHTEN |
| Package Description | 30 mL in 1 TUBE (54272-201-11) |
| Product NDC | 54272-201 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ZINC OXIDE OCTINOXATE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20130221 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | CEN BEAUTY LLC |
| Substance Name | OCTINOXATE; ZINC OXIDE |
| Strength Number | 6; 15 |
| Strength Unit | g/100mL; g/100mL |
| Pharmaceutical Classes |
