Product NDC: | 58414-2500 |
Proprietary Name: | NeoCeuticals |
Non Proprietary Name: | HYDROQUINONE |
Active Ingredient(s): | .02 g/g & nbsp; HYDROQUINONE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 58414-2500 |
Labeler Name: | NeoStrata Company Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part358A |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110222 |
Package NDC: | 58414-2500-1 |
Package Description: | 1 TUBE in 1 CARTON (58414-2500-1) > 30 g in 1 TUBE |
NDC Code | 58414-2500-1 |
Proprietary Name | NeoCeuticals |
Package Description | 1 TUBE in 1 CARTON (58414-2500-1) > 30 g in 1 TUBE |
Product NDC | 58414-2500 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | HYDROQUINONE |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 20110222 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | NeoStrata Company Inc |
Substance Name | HYDROQUINONE |
Strength Number | .02 |
Strength Unit | g/g |
Pharmaceutical Classes |