Cornex - 56104-009-15 - (Corn and Callus Liquid Remover)

Alphabetical Index


Drug Information of Cornex

Product NDC: 56104-009
Proprietary Name: Cornex
Non Proprietary Name: Corn and Callus Liquid Remover
Active Ingredient(s): .17    g/g & nbsp;   Corn and Callus Liquid Remover
Administration Route(s): TOPICAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Cornex

Product NDC: 56104-009
Labeler Name: Premier Brands of America Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part358F
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20130101

Package Information of Cornex

Package NDC: 56104-009-15
Package Description: 15 g in 1 BOTTLE, WITH APPLICATOR (56104-009-15)

NDC Information of Cornex

NDC Code 56104-009-15
Proprietary Name Cornex
Package Description 15 g in 1 BOTTLE, WITH APPLICATOR (56104-009-15)
Product NDC 56104-009
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Corn and Callus Liquid Remover
Dosage Form Name LIQUID
Route Name TOPICAL
Start Marketing Date 20130101
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Premier Brands of America Inc.
Substance Name SALICYLIC ACID
Strength Number .17
Strength Unit g/g
Pharmaceutical Classes

Complete Information of Cornex


General Information