esika - 13537-505-01 - (Aluminum Chlorohydrate)

Alphabetical Index


Drug Information of esika

Product NDC: 13537-505
Proprietary Name: esika
Non Proprietary Name: Aluminum Chlorohydrate
Active Ingredient(s): .045    g/mL & nbsp;   Aluminum Chlorohydrate
Administration Route(s): TOPICAL
Dosage Form(s): SPRAY
Coding System: National Drug Codes(NDC)

Labeler Information of esika

Product NDC: 13537-505
Labeler Name: Ventura Corporation LTD.
Product Type: HUMAN OTC DRUG
FDA Application Number: part350
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20130527

Package Information of esika

Package NDC: 13537-505-01
Package Description: 125 mL in 1 BOTTLE, SPRAY (13537-505-01)

NDC Information of esika

NDC Code 13537-505-01
Proprietary Name esika
Package Description 125 mL in 1 BOTTLE, SPRAY (13537-505-01)
Product NDC 13537-505
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Aluminum Chlorohydrate
Dosage Form Name SPRAY
Route Name TOPICAL
Start Marketing Date 20130527
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Ventura Corporation LTD.
Substance Name ALUMINUM CHLOROHYDRATE
Strength Number .045
Strength Unit g/mL
Pharmaceutical Classes

Complete Information of esika


General Information