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BRIGHTEN
BRIGHTEN - 54272-301-11 - (HYDROQUINONE)
Drug Information of BRIGHTEN
| Product NDC: | 54272-301 |
| Proprietary Name: | BRIGHTEN |
| Non Proprietary Name: | HYDROQUINONE |
| Active Ingredient(s): | 2 g/100mL & nbsp; HYDROQUINONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of BRIGHTEN
| Product NDC: | 54272-301 |
| Labeler Name: | CEN BEAUTY LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part358A |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130221 |
Package Information of BRIGHTEN
| Package NDC: | 54272-301-11 |
| Package Description: | 30 mL in 1 TUBE (54272-301-11) |
NDC Information of BRIGHTEN
| NDC Code | 54272-301-11 |
| Proprietary Name | BRIGHTEN |
| Package Description | 30 mL in 1 TUBE (54272-301-11) |
| Product NDC | 54272-301 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | HYDROQUINONE |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20130221 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | CEN BEAUTY LLC |
| Substance Name | HYDROQUINONE |
| Strength Number | 2 |
| Strength Unit | g/100mL |
| Pharmaceutical Classes |
