Product NDC: | 51545-120 |
Proprietary Name: | Porcelana Night Skin Lightening |
Non Proprietary Name: | Hydroquinone |
Active Ingredient(s): | .02 g/g & nbsp; Hydroquinone |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51545-120 |
Labeler Name: | Ultimark Products LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part358A |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110401 |
Package NDC: | 51545-120-03 |
Package Description: | 1 JAR in 1 BOX (51545-120-03) > 85 g in 1 JAR |
NDC Code | 51545-120-03 |
Proprietary Name | Porcelana Night Skin Lightening |
Package Description | 1 JAR in 1 BOX (51545-120-03) > 85 g in 1 JAR |
Product NDC | 51545-120 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Hydroquinone |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20110401 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Ultimark Products LLC |
Substance Name | HYDROQUINONE |
Strength Number | .02 |
Strength Unit | g/g |
Pharmaceutical Classes |