VIONEXUS- alcohol 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]

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 cause disease
• helps prevent cross contamination by hand contact
• helps prevent drying and chafing of skin
• recmmended for repeated use

Active ingredients

Ethanol 72%v/v

Purpose

Antiseptic

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 ambient temperature
• 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.

Case Label

INGREDIENTS AND APPEARANCE

VIONEXUS 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55443-0401
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	72 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55443-0401-2	12 in 1 CASE	03/30/2020
1	NDC: 55443-0401-1	237 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
2	NDC: 55443-0401-4	12 in 1 CASE	04/06/2020
2	NDC: 55443-0401-3	710 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/30/2020

Labeler - METREX RESEARCH (102567567)

Registrant - METREX RESEARCH (102567567)

Establishment
Name	Address	ID/FEI	Business Operations
METREX RESEARCH		102567567	label(55443-0401)

Establishment
Name	Address	ID/FEI	Business Operations
METREX RESEARCH		145963778	manufacture(55443-0401)