Product NDC: | 66129-210 |
Proprietary Name: | Crusader Ultra Skin Lightening |
Non Proprietary Name: | HYDROQUINONE |
Active Ingredient(s): | 1.14; .285 g/57g; g/57g & nbsp; HYDROQUINONE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 66129-210 |
Labeler Name: | International Beauty Exchange |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part358A |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110101 |
Package NDC: | 66129-210-39 |
Package Description: | 57 g in 1 TUBE (66129-210-39) |
NDC Code | 66129-210-39 |
Proprietary Name | Crusader Ultra Skin Lightening |
Package Description | 57 g in 1 TUBE (66129-210-39) |
Product NDC | 66129-210 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | HYDROQUINONE |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20110101 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | International Beauty Exchange |
Substance Name | HYDROQUINONE; PADIMATE O |
Strength Number | 1.14; .285 |
Strength Unit | g/57g; g/57g |
Pharmaceutical Classes |