VIONEXUS- chloroxylenol liquid

VioNexus by

Drug Labeling and Warnings

VioNexus by is a Otc medication manufactured, distributed, or labeled by Metrex Research. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Principal Display Panel

VioNexus
no-rinse spray

Antiseptic Handwash

Metrex
Protecting People

MADE IN USA

Contents:
x Liter
x fl. oz.
x mL


Manufactured By:
METREX RESEARCH CORPORATION
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

Uses

• 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
  

Warnings

• 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.

Directions

• 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 Ingredients

Acetone, 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 www.metrex.com.

PRINCIPAL DISPLAY PANEL

image of VioNexusNRSBottle 

image of VioNexusNRSBox 

INGREDIENTS AND APPEARANCE

VIONEXUS 
chloroxylenol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55443-0200
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.085 g  in 100 mL
ETHANOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ETHANOL	77.01 g  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55443-0200-5	48 in 1 CASE
1	NDC: 55443-0200-1	59 mL in 1 BOTTLE, PLASTIC
2	NDC: 55443-0200-4	3 in 1 CASE
2	NDC: 55443-0200-3	2 in 1 BOX
2	NDC: 55443-0200-2	1000 mL in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	01/01/1992

Labeler - Metrex Research (102567567)