Home > National Drug Code (NDC) > ANTIMICROBIAL FOAMING

ANTIMICROBIAL FOAMING - 63148-241-12 - (BENZETHONIUM CHLORIDE)

Alphabetical Index


Drug Information of ANTIMICROBIAL FOAMING

Product NDC: 63148-241
Proprietary Name: ANTIMICROBIAL FOAMING
Non Proprietary Name: BENZETHONIUM CHLORIDE
Active Ingredient(s): .1    mL/100mL & nbsp;   BENZETHONIUM CHLORIDE
Administration Route(s): TOPICAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of ANTIMICROBIAL FOAMING

Product NDC: 63148-241
Labeler Name: APOLLO HEALTH AND BEAUTY CARE
Product Type: HUMAN OTC DRUG
FDA Application Number: part333E
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20110722

Package Information of ANTIMICROBIAL FOAMING

Package NDC: 63148-241-12
Package Description: 354 mL in 1 BOTTLE (63148-241-12)

NDC Information of ANTIMICROBIAL FOAMING

NDC Code 63148-241-12
Proprietary Name ANTIMICROBIAL FOAMING
Package Description 354 mL in 1 BOTTLE (63148-241-12)
Product NDC 63148-241
Product Type Name HUMAN OTC DRUG
Non Proprietary Name BENZETHONIUM CHLORIDE
Dosage Form Name LIQUID
Route Name TOPICAL
Start Marketing Date 20110722
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name APOLLO HEALTH AND BEAUTY CARE
Substance Name BENZETHONIUM CHLORIDE
Strength Number .1
Strength Unit mL/100mL
Pharmaceutical Classes

Complete Information of ANTIMICROBIAL FOAMING


General Information