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Superlightener
Superlightener - 66915-413-04 - (Hydroquinone)
Drug Information of Superlightener
| 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) |
Labeler Information of Superlightener
| 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 Information of Superlightener
| Package NDC: | 66915-413-04 |
| Package Description: | 1 BOTTLE, GLASS in 1 CARTON (66915-413-04) > 30 g in 1 BOTTLE, GLASS (66915-413-03) |
NDC Information of Superlightener
| NDC Code | 66915-413-04 |
| Proprietary Name | Superlightener |
| Package Description | 1 BOTTLE, GLASS in 1 CARTON (66915-413-04) > 30 g in 1 BOTTLE, GLASS (66915-413-03) |
| 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 |
