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Medically reviewed on August 30, 2017

Dosage form: liquid
Ingredients: BENZALKONIUM CHLORIDE 0.085g in 100mL, ETHANOL 77.01g in 100mL
Labeler: Metrex Research
NDC Code: 55443-0200

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.

VioNexus No Rinse Spray

Principal Display PanelVioNexus
no-rinse spray

Antiseptic Handwash

Protecting People


x Liter
x fl. oz.
x mL

Manufactured By:
1717 W. Collins Avenue
Orange, CA 92867

Imported By:
Sybron Canada LP
Brampton, Ontario L6W 4T5

Drug Facts Active ingredients                                        Purpose
Benzalkonium Chloride 0.10%/wt .......................Antiseptic handwash
Ethanol 65.87%/wt ............................................Antiseptic handwash

  • for handwashing to decrease bacteria on the skin
  • helps prevent cross contamination by hand contact
  • helps prevent drying and chafing of skin
  • recommended for repeated use

  • For external use only
  • Flammable, keep away from fire or flame

When using this product

  • do not use in or near eyes
  • use in a well-ventilated area
  • discontinue use if irritation and redness develop

Keep out of reach of children

In case of accidental ingestion, seek medical attention or contact a poison control center immediately.

  • wet hands thoroughly with spray, covering entire surface of hands, including fingertips and cuticles
  • rub vigorously into skin until dry
  • no rinsing or wiping is required

Other information

  • store in a dry, cool place below 104 F
  • recommended for use in the VioNexus No-Touch Dispenser
  • for hospital and professional use only

Inactive IngredientsAcetone, glycerin, purified water

Questions or comments?For product or technical information, contact Metrex, Monday-Friday, 6am-4pm PST at 800-841-1428 or visit our website at

image of VioNexusNRSBottle 

image of VioNexusNRSBox 
chloroxylenol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55443-0200
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
#Item CodePackage Description
1NDC:55443-0200-548 BOTTLE, PLASTIC (BOTTLE) in 1 CASE
1NDC:55443-0200-159 mL in 1 BOTTLE, PLASTIC
2NDC:55443-0200-43 BOX (BOX) in 1 CASE
2NDC:55443-0200-32 BOTTLE, PLASTIC (BOTTLE) in 1 BOX
2NDC:55443-0200-21000 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E01/01/1992
Labeler - Metrex Research (102567567)

Metrex Research

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.