Home > National Drug Code (NDC) > Crusader Ultra Skin Lightening

Crusader Ultra Skin Lightening - 66129-210-39 - (HYDROQUINONE)

Alphabetical Index


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

Complete Information of Crusader Ultra Skin Lightening


General Information