Product NDC: | 45802-982 |
Proprietary Name: | Perrigo Hydroquinone |
Non Proprietary Name: | Hydroquinone |
Active Ingredient(s): | 30; 40; 50 mg/g; mg/g; mg/g & nbsp; Hydroquinone |
Administration Route(s): | TOPICAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 45802-982 |
Labeler Name: | Perrigo New York Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20090204 |
Package NDC: | 45802-982-64 |
Package Description: | 1 TUBE in 1 CARTON (45802-982-64) > 28.35 g in 1 TUBE |
NDC Code | 45802-982-64 |
Proprietary Name | Perrigo Hydroquinone |
Package Description | 1 TUBE in 1 CARTON (45802-982-64) > 28.35 g in 1 TUBE |
Product NDC | 45802-982 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Hydroquinone |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 20090204 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Perrigo New York Inc |
Substance Name | DIOXYBENZONE; HYDROQUINONE; PADIMATE O |
Strength Number | 30; 40; 50 |
Strength Unit | mg/g; mg/g; mg/g |
Pharmaceutical Classes | Depigmenting Activity [PE],Melanin Synthesis Inhibitor [EPC],Melanin Synthesis Inhibitors [MoA] |