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Sunvanish
Sunvanish - 64760-201-01 - (Hydroquinone)
Drug Information of Sunvanish
| Product NDC: | 64760-201 |
| Proprietary Name: | Sunvanish |
| Non Proprietary Name: | Hydroquinone |
| Active Ingredient(s): | 40 mg/g & nbsp; Hydroquinone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sunvanish
| Product NDC: | 64760-201 |
| Labeler Name: | Glytone |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | part358A |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20091001 |
Package Information of Sunvanish
| Package NDC: | 64760-201-01 |
| Package Description: | 1 TUBE in 1 BOX (64760-201-01) > 56 g in 1 TUBE |
NDC Information of Sunvanish
| NDC Code | 64760-201-01 |
| Proprietary Name | Sunvanish |
| Package Description | 1 TUBE in 1 BOX (64760-201-01) > 56 g in 1 TUBE |
| Product NDC | 64760-201 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hydroquinone |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20091001 |
| 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] |
