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Durisan Antimicrobial

Medically reviewed by Drugs.com. Last updated on Oct 21, 2021.

Dosage form: liquid
Ingredients: BENZALKONIUM CHLORIDE 2.5mg in 250mL
Labeler: Sanit Technologies LLC
NDC Code: 71120-612

Durisan - 612

Drug Facts
Active Ingredient

Benzalkonium Chloride 0.1%

Purpose

Antiseptic

Use:

For handwashing to decrease bacteria on the skin.

Warnings:

For external use only.

When using theis product, avoid contact with eyes. In case of contact, flush with water.

Stop use

and ask a doctor if irritation or redness develops.

Keep out of reach of children except under adult supervision.

If swallowed, get medical help or contact a poison control center immediately.

Directions:

Pump into dry skin. Lather vigorously for 15 seconds. Rinse and dry thoroughly.

Inactive Ingredients:

Deionized water, disodium EDTA, cocoamidopropyl betadine, glycerin, centrimoniun chloride, benzoic acid, sorbic acid.

Durisan Antimicrobial product label

Durisan™

Antimicrobial
Liquid Hand Soap
Gentle on skin for healthier skin.

Alcohol Fre

Antibacterial properties - lasts long
Kills more germs than other liquid hand soaps

MADE IN THE USA WITH PRIDE

POWERED BY
SANIT TECHNOLOGIES LLC

550 ml
NET WT 19 oz

Sanit Technologies LLC
7810 25th Court East
Sarasota, Florida 34243
Tel: 844-DURISAN
www.santitechnologies.com
844-DURISAN
sanittechnologies.com

DURISAN  ANTIMICROBIAL
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71120-612
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE2.5 mg  in 250 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
EDETATE DISODIUM ANHYDROUS 
COCAMIDOPROPYL BETAINE 
GLYCERIN 
CETRIMONIUM CHLORIDE 
BENZOIC ACID 
SORBIC ACID 
Packaging
#Item CodePackage Description
1NDC:71120-612-01550 mL in 1 BOTTLE, PUMP
2NDC:71120-612-0250 mL in 1 PACKAGE
3NDC:71120-612-03250 mL in 1 PACKAGE
4NDC:71120-612-04550 mL in 1 PACKAGE
5NDC:71120-612-051000 mL in 1 PACKAGE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E01/01/2016
Labeler - Sanit Technologies LLC (075711022)
Registrant - Sanit Technologies LLC (075711022)

 
Sanit Technologies LLC

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.