Product NDC: | 68788-9916 |
Proprietary Name: | Hydroquinone |
Non Proprietary Name: | HYDROQUINONE, DIOXYBENZONE, OXYBENZONE, PADIMATE O |
Active Ingredient(s): | 30; 40; 20; 80 mg/g; mg/g; mg/g; mg/g & nbsp; HYDROQUINONE, DIOXYBENZONE, OXYBENZONE, PADIMATE O |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68788-9916 |
Labeler Name: | Preferred Pharmaceuticals, Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20120130 |
Package NDC: | 68788-9916-2 |
Package Description: | 1 TUBE in 1 CARTON (68788-9916-2) > 28.35 g in 1 TUBE |
NDC Code | 68788-9916-2 |
Proprietary Name | Hydroquinone |
Package Description | 1 TUBE in 1 CARTON (68788-9916-2) > 28.35 g in 1 TUBE |
Product NDC | 68788-9916 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | HYDROQUINONE, DIOXYBENZONE, OXYBENZONE, PADIMATE O |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20120130 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Preferred Pharmaceuticals, Inc |
Substance Name | DIOXYBENZONE; HYDROQUINONE; OXYBENZONE; PADIMATE O |
Strength Number | 30; 40; 20; 80 |
Strength Unit | mg/g; mg/g; mg/g; mg/g |
Pharmaceutical Classes | Depigmenting Activity [PE],Melanin Synthesis Inhibitor [EPC],Melanin Synthesis Inhibitors [MoA] |