Ban - 10596-339-35 - (Aluminum Chlorohydrate)

Alphabetical Index


Drug Information of Ban

Product NDC: 10596-339
Proprietary Name: Ban
Non Proprietary Name: Aluminum Chlorohydrate
Active Ingredient(s): 20    g/103mL & nbsp;   Aluminum Chlorohydrate
Administration Route(s): TOPICAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Ban

Product NDC: 10596-339
Labeler Name: Kao Brands Company
Product Type: HUMAN OTC DRUG
FDA Application Number: part350
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20120101

Package Information of Ban

Package NDC: 10596-339-35
Package Description: 103 mL in 1 BOTTLE, WITH APPLICATOR (10596-339-35)

NDC Information of Ban

NDC Code 10596-339-35
Proprietary Name Ban
Package Description 103 mL in 1 BOTTLE, WITH APPLICATOR (10596-339-35)
Product NDC 10596-339
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Aluminum Chlorohydrate
Dosage Form Name LIQUID
Route Name TOPICAL
Start Marketing Date 20120101
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Kao Brands Company
Substance Name ALUMINUM CHLOROHYDRATE
Strength Number 20
Strength Unit g/103mL
Pharmaceutical Classes

Complete Information of Ban


General Information