Product NDC: | 64760-202 |
Proprietary Name: | Glytone Clarifying |
Non Proprietary Name: | Hydroquinone |
Active Ingredient(s): | 40 mg/g & nbsp; Hydroquinone |
Administration Route(s): | TOPICAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 64760-202 |
Labeler Name: | Glytone |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | part358A |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20101109 |
Package NDC: | 64760-202-01 |
Package Description: | 1 TUBE in 1 BOX (64760-202-01) > 56 g in 1 TUBE |
NDC Code | 64760-202-01 |
Proprietary Name | Glytone Clarifying |
Package Description | 1 TUBE in 1 BOX (64760-202-01) > 56 g in 1 TUBE |
Product NDC | 64760-202 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Hydroquinone |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 20101109 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Glytone |
Substance Name | HYDROQUINONE |
Strength Number | 40 |
Strength Unit | mg/g |
Pharmaceutical Classes | Depigmenting Activity [PE],Melanin Synthesis Inhibitor [EPC],Melanin Synthesis Inhibitors [MoA] |