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Crusader Ultra Skin Lightening
Crusader Ultra Skin Lightening - 66129-210-39 - (HYDROQUINONE)
Drug Information of Crusader Ultra Skin Lightening
| 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) |
Labeler Information of Crusader Ultra Skin Lightening
| 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 Information of Crusader Ultra Skin Lightening
| Package NDC: | 66129-210-39 |
| Package Description: | 57 g in 1 TUBE (66129-210-39) |
NDC Information of Crusader Ultra Skin Lightening
| 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 |
