ESIKA - 13537-134-01 - (Aluminum Sesquichlorohydrate)

Alphabetical Index


Drug Information of ESIKA

Product NDC: 13537-134
Proprietary Name: ESIKA
Non Proprietary Name: Aluminum Sesquichlorohydrate
Active Ingredient(s): .17    g/mL & nbsp;   Aluminum Sesquichlorohydrate
Administration Route(s): TOPICAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of ESIKA

Product NDC: 13537-134
Labeler Name: Ventura Corporation Ltd.
Product Type: HUMAN OTC DRUG
FDA Application Number: part350
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20111213

Package Information of ESIKA

Package NDC: 13537-134-01
Package Description: 50 mL in 1 BOTTLE (13537-134-01)

NDC Information of ESIKA

NDC Code 13537-134-01
Proprietary Name ESIKA
Package Description 50 mL in 1 BOTTLE (13537-134-01)
Product NDC 13537-134
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Aluminum Sesquichlorohydrate
Dosage Form Name LIQUID
Route Name TOPICAL
Start Marketing Date 20111213
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Ventura Corporation Ltd.
Substance Name ALUMINUM SESQUICHLOROHYDRATE
Strength Number .17
Strength Unit g/mL
Pharmaceutical Classes

Complete Information of ESIKA


General Information