Azuro - 49955-100-50 - (ALCOHOL)

Alphabetical Index

Drug Information of Azuro

Product NDC: 49955-100
Proprietary Name: Azuro
Non Proprietary Name: ALCOHOL
Active Ingredient(s): .7    L/L & nbsp;   ALCOHOL
Administration Route(s): TOPICAL
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of Azuro

Product NDC: 49955-100
Labeler Name: Noveko Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part333
Start Marketing Date: 20091118

Package Information of Azuro

Package NDC: 49955-100-50
Package Description: .5 L in 1 BOTTLE (49955-100-50)

NDC Information of Azuro

NDC Code 49955-100-50
Proprietary Name Azuro
Package Description .5 L in 1 BOTTLE (49955-100-50)
Product NDC 49955-100
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ALCOHOL
Dosage Form Name GEL
Route Name TOPICAL
Start Marketing Date 20091118
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Noveko Inc
Substance Name ALCOHOL
Strength Number .7
Strength Unit L/L
Pharmaceutical Classes

Complete Information of Azuro

General Information