DURISAN  ANTIMICROBIAL- benzalkonium chloride liquid 
Sanit Technologies LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Durisan - 612

Drug Facts
Active Ingredient

Benzalkonium Chloride 0.1%

Purpose

Antiseptic

Use:

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 consult a doctor if irritation or redness develops.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

Directions:

  • Pump onto dry skin. Lather vigorously for 20 seconds.
  • Rinse hands and dry thoroughly.

Inactive Ingredients:

water, cocamidopropyl betaine, glycerin, cetrimonium chloride, benzyl alcohol, disodium EDTA, benzoic acid, sorbic acid

Product label

Durisan ®

Antimicrobial

Liquid Hand Soap

MADE IN THE USA WITH PRIDE

POWERED BY
SANIT TECHNOLOGIES LLC

550 mL
Net Content 18.59 oz

Sanit Technologies LLC
7810 25th Court East Unit 106
Sarasota, Florida 34243

Tel. 941.351.9114

www.DURISAN.com

image description

DURISAN   ANTIMICROBIAL
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71120-612
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE2.5 mg  in 250 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
GLYCERIN (UNII: PDC6A3C0OX)  
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
BENZOIC ACID (UNII: 8SKN0B0MIM)  
SORBIC ACID (UNII: X045WJ989B)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71120-612-01550 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product01/01/201610/20/2020
2NDC:71120-612-0250 mL in 1 PACKAGE; Type 0: Not a Combination Product01/01/201611/23/2020
3NDC:71120-612-03250 mL in 1 PACKAGE; Type 0: Not a Combination Product01/01/201611/23/2020
4NDC:71120-612-04550 mL in 1 PACKAGE; Type 0: Not a Combination Product01/01/201611/23/2020
5NDC:71120-612-051000 mL in 1 PACKAGE; Type 0: Not a Combination Product01/01/201611/23/2020
6NDC:71120-612-06118 mL in 1 PACKAGE; Type 0: Not a Combination Product01/01/201611/23/2020
7NDC:71120-612-07236.58 mL in 1 PACKAGE; Type 0: Not a Combination Product01/01/201611/23/2020
8NDC:71120-612-08300 mL in 1 PACKAGE; Type 0: Not a Combination Product01/01/201611/23/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E01/01/201611/23/2020
Labeler - Sanit Technologies LLC (075711022)
Registrant - Sanit Technologies LLC (075711022)

Revised: 2/2021
 
Sanit Technologies LLC