Product NDC: | 58980-580 |
Proprietary Name: | Alphaquin HP |
Non Proprietary Name: | Hydroquinone, Octinoxate, and Oxybenzone |
Active Ingredient(s): | 40; 75; 50 mg/g; mg/g; mg/g & nbsp; Hydroquinone, Octinoxate, and Oxybenzone |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 58980-580 |
Labeler Name: | Stratus Pharamceuticals |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 19930101 |
Package NDC: | 58980-580-10 |
Package Description: | 1 TUBE in 1 BOX (58980-580-10) > 28.4 g in 1 TUBE |
NDC Code | 58980-580-10 |
Proprietary Name | Alphaquin HP |
Package Description | 1 TUBE in 1 BOX (58980-580-10) > 28.4 g in 1 TUBE |
Product NDC | 58980-580 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Hydroquinone, Octinoxate, and Oxybenzone |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 19930101 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Stratus Pharamceuticals |
Substance Name | HYDROQUINONE; OCTINOXATE; OXYBENZONE |
Strength Number | 40; 75; 50 |
Strength Unit | mg/g; mg/g; mg/g |
Pharmaceutical Classes | Depigmenting Activity [PE],Melanin Synthesis Inhibitor [EPC],Melanin Synthesis Inhibitors [MoA] |