VioNexus No Rinse Spray

Manufacturer
METREX RESEARCH, LLC | METREX RESEARCH
Effective date
2026-10-05
Label type
HUMAN OTC DRUG LABEL
Version
12
Source
daily-update
Hydrated at
2026-10-09 01:01:43

Label at a glance#

ProductVIONEXUS
Active ingredientALCOHOL
Label structure9 sections

Indications and 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

Dosage and administration

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

Storage and handling

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

Label contents#

Full prescribing information#

Warnings

WARNINGS SECTION

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

When using this product

OTC - WHEN USING SECTION

  • do not use in or near eyes
  • discontinue use if irritation and redness develop

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Uses

INDICATIONS & USAGE SECTION

  • 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

OTC - ACTIVE INGREDIENT SECTION

Ethanol 72%v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic Hand Rub

Directions

INSTRUCTIONS FOR USE SECTION

  • 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

STORAGE AND HANDLING SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified water, isopropanol, glycerin

Questions or comments?

OTC - QUESTIONS SECTION

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)

DOSAGE & ADMINISTRATION SECTION

  • 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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

VioNexus No Rinse Spray 1L LabelVioNexus No Rinse Spray 1L LabelVioNexus No Rinse Spray 2oz LabelVioNexus No Rinse Spray 2oz LabelVioNexus Antiseptic Hand Rub

No-Rinse Spray

Metrex

Contents

Made in the US

NDC 55443-0400

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55443-040055443-0400-1, 55443-0400-5, 55443-0400-2, 55443-0400-3, 55443-0400-4, 55443-0400-6, 55443-0400-7

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Source Document#

Source XML · Source PDF

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
112026-04-28full-release2026-06-01 01:55:25

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
VIONEXUSALCOHOLMETREX RESEARCH, LLC7542cf97-05fa-18e3-e053-2991aa0ac7eb2026-04-28WarningsExact identifier
ndc (package): 55443-0400-2
ndc (package): 55443-0400-5
ndc (package): 55443-0400-7
ndc (package): 55443-0400-4
ndc (package): 55443-0400-3
ndc (package): 55443-0400-6
ndc (package): 55443-0400-1
ndc (product): 55443-0400
ndc11 (package): 55443040007
ndc11 (package): 55443040004
ndc11 (package): 55443040001
ndc11 (package): 55443040005
ndc11 (package): 55443040002
ndc11 (package): 55443040003
ndc11 (package): 55443040006
spl set id: 7542cf97-05fa-18e3-e053-2991aa0ac7eb

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.