Aclaro - 68712-003-01 - (Hydroquinone)

Alphabetical Index


Drug Information of Aclaro

Product NDC: 68712-003
Proprietary Name: Aclaro
Non Proprietary Name: Hydroquinone
Active Ingredient(s): 40    mg/g & nbsp;   Hydroquinone
Administration Route(s): TOPICAL
Dosage Form(s): EMULSION
Coding System: National Drug Codes(NDC)

Labeler Information of Aclaro

Product NDC: 68712-003
Labeler Name: Innocutis
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20040601

Package Information of Aclaro

Package NDC: 68712-003-01
Package Description: 48.2 g in 1 BOTTLE, PUMP (68712-003-01)

NDC Information of Aclaro

NDC Code 68712-003-01
Proprietary Name Aclaro
Package Description 48.2 g in 1 BOTTLE, PUMP (68712-003-01)
Product NDC 68712-003
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydroquinone
Dosage Form Name EMULSION
Route Name TOPICAL
Start Marketing Date 20040601
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Innocutis
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 Aclaro


General Information