VioNexus No Rinse Spray

VioNexus No Rinse Spray

Drug Labeling and Warnings

Drug Details

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VIONEXUS- alcohol liquid 
METREX RESEARCH, 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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VioNexus No Rinse Spray

Warnings

  • For external use only
  • Flammable, keep away from fire or flame
  • Do not ingest

When using this product

  • do not use in or near eyes
  • 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.

Uses

  • to help reduce bacteria that potentially can case disease
  • helps prevent cross contamination by hand contact
  • helps prevent drying and chafing of skin
  • recommended for repeated use

Active ingredients

Ethanol 72%v/v

Purpose

Antiseptic Hand Rub

Directions

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

Other information

  • store at room temperature
  • recommended for us in the Vionexus No-Touch Dispenser
  • for healthcare and professional use only

Inactive ingredients

Purified water, isopropanol, glycerin

Questions or comments?

For product or technical information, contact Metrex, Monday to Friday, 6am - 4pm PST at 800-841-1428 or visit our website at www.metrex.com.

Dosage and Administration Route(s)

  • Administration Route(s): Topical - Administration to a particular spot on the outer surface of the body.
  • Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid state.

Vionexus No Rinse Spray Label

Vionexus No Rinse Spray 2 Ounce Case Vionexus No Rinse Spray 1 Liter CaseVionexus No Rinse Spray 1 Liter Box Vionexus No Rinse Spray 1 Liter BottleVionexus No Rinse Spray 2 Ounce Bottle

VIONEXUS 
alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 55443-0400
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL72 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
Product Characteristics
Color    Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 55443-0400-548 in 1 CASE11/01/2018
1NDC: 55443-0400-159 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
2NDC: 55443-0400-43 in 1 CASE11/01/2018
2NDC: 55443-0400-32 in 1 BOX
2NDC: 55443-0400-21000 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product
Image of Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E11/01/2018
Labeler - METREX RESEARCH, LLC (102567567)
Registrant - METREX RESEARCH (102567567)
Establishment
NameAddressID/FEIBusiness Operations
Metrex Research102567567label(55443-0400)
Establishment
NameAddressID/FEIBusiness Operations
METREX RESEARCH145963778manufacture(55443-0400)

Revised: 9/2019
 
METREX RESEARCH, LLC


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