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NU-DERM BLENDER - 62032-100-10 - (HYDROQUINONE)

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Drug Information of NU-DERM BLENDER

Product NDC: 62032-100
Proprietary Name: NU-DERM BLENDER
Non Proprietary Name: HYDROQUINONE
Active Ingredient(s): 40    mg/g & nbsp;   HYDROQUINONE
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of NU-DERM BLENDER

Product NDC: 62032-100
Labeler Name: OMP, INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 19880101

Package Information of NU-DERM BLENDER

Package NDC: 62032-100-10
Package Description: 28.5 g in 1 BOTTLE, PLASTIC (62032-100-10)

NDC Information of NU-DERM BLENDER

NDC Code 62032-100-10
Proprietary Name NU-DERM BLENDER
Package Description 28.5 g in 1 BOTTLE, PLASTIC (62032-100-10)
Product NDC 62032-100
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name HYDROQUINONE
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 19880101
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name OMP, INC.
Substance Name HYDROQUINONE
Strength Number 40
Strength Unit mg/g
Pharmaceutical Classes Depigmenting Activity [PE],Melanin Synthesis Inhibitor [EPC],Melanin Synthesis Inhibitors [MoA]

Complete Information of NU-DERM BLENDER


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