DURISAN ANTIMICROBIAL- benzalkonium chloride liquid

Durisan by

Drug Labeling and Warnings

Durisan by is a Otc medication manufactured, distributed, or labeled by Sanit Technologies LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug FactsActive 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

INGREDIENTS AND APPEARANCE

DURISAN  ANTIMICROBIAL
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71120-612
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	2.5 mg  in 250 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
GLYCERIN (UNII: PDC6A3C0OX)
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
BENZOIC ACID (UNII: 8SKN0B0MIM)
SORBIC ACID (UNII: X045WJ989B)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71120-612-01	550 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	01/01/2016
2	NDC: 71120-612-02	50 mL in 1 PACKAGE; Type 0: Not a Combination Product	01/01/2016
3	NDC: 71120-612-03	250 mL in 1 PACKAGE; Type 0: Not a Combination Product	01/01/2016
4	NDC: 71120-612-04	550 mL in 1 PACKAGE; Type 0: Not a Combination Product	01/01/2016
5	NDC: 71120-612-05	1000 mL in 1 PACKAGE; Type 0: Not a Combination Product	01/01/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	01/01/2016

Labeler - Sanit Technologies LLC (075711022)

Registrant - Sanit Technologies LLC (075711022)