Product NDC: | 66915-413 |
Proprietary Name: | Superlightener |
Non Proprietary Name: | Hydroquinone |
Active Ingredient(s): | 20 mg/g & nbsp; Hydroquinone |
Administration Route(s): | TOPICAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 66915-413 |
Labeler Name: | CoValence Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part358A |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20100701 |
Package NDC: | 66915-413-17 |
Package Description: | 30 g in 1 BOTTLE, GLASS (66915-413-17) |
NDC Code | 66915-413-17 |
Proprietary Name | Superlightener |
Package Description | 30 g in 1 BOTTLE, GLASS (66915-413-17) |
Product NDC | 66915-413 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Hydroquinone |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 20100701 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | CoValence Inc |
Substance Name | HYDROQUINONE |
Strength Number | 20 |
Strength Unit | mg/g |
Pharmaceutical Classes |