KANKA - 10157-9493-1 - (Benzocaine and Zinc Chloride)

Alphabetical Index


Drug Information of KANKA

Product NDC: 10157-9493
Proprietary Name: KANKA
Non Proprietary Name: Benzocaine and Zinc Chloride
Active Ingredient(s): 20; .1    mL/100g; g/100g & nbsp;   Benzocaine and Zinc Chloride
Administration Route(s): ORAL
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of KANKA

Product NDC: 10157-9493
Labeler Name: Blistex Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part356
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20090501

Package Information of KANKA

Package NDC: 10157-9493-1
Package Description: 1 APPLICATOR in 1 BLISTER PACK (10157-9493-1) > 2 g in 1 APPLICATOR

NDC Information of KANKA

NDC Code 10157-9493-1
Proprietary Name KANKA
Package Description 1 APPLICATOR in 1 BLISTER PACK (10157-9493-1) > 2 g in 1 APPLICATOR
Product NDC 10157-9493
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Benzocaine and Zinc Chloride
Dosage Form Name GEL
Route Name ORAL
Start Marketing Date 20090501
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Blistex Inc.
Substance Name BENZOCAINE; ZINC CHLORIDE
Strength Number 20; .1
Strength Unit mL/100g; g/100g
Pharmaceutical Classes

Complete Information of KANKA


General Information