Label: VIONEXUS- chloroxylenol liquid

  • NDC Code(s): 55443-0600-1, 55443-0600-2, 55443-0600-3
  • Packager: Metrex Research, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 6, 2023

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  • Drug Facts

    1L Whole LabelActive Ingredients Purpose

    Chloroxylenol 1.0%................Healthcare personnel handwash

    Uses

    • handwash to help reduce bacteria that potentially can cause disease
    • helps prevent cross contamination by hand contact
    • recommended for repeated use

    Warnings

    For external use only

    Keep out of reach of children

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

    Directions

    • wet hands and forearms
    • apply 5-10 ml to hands and forearms
    • scrub thoroughly for at least 30 seconds and include fingertips and cuticles
    • rinse

    Inactive Ingredients

    D&C Green 5, D&C Green 8, fragrance, potassium cocoate, purified water, tetrasodium EDTA

    Healthcare Personnel Handwash

  • Principal Display Panel

    1L Front Panel

    VioNexus

    antimicrobial foaming soap

    Healthcare Personnel Handwash

    Manufactured for:

    METREX RESEARCH

    28210 Wick Road

    Romulus, Michigan 48174

    Reorder No.:

    Metrex

    Protecting People

    Contents: 1 Liter

  • PRINCIPAL DISPLAY PANEL

    Case Label

  • PRINCIPAL DISPLAY PANEL

    Inner Box

  • INGREDIENTS AND APPEARANCE
    VIONEXUS 
    chloroxylenol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55443-0600
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL1 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    D&C GREEN NO. 8 (UNII: I2W85YOX9L)  
    D&C GREEN NO. 5 (UNII: 8J6RDU8L9X)  
    POTASSIUM COCOATE (UNII: F8U72V8ZXP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:55443-0600-33 in 1 CASE10/01/2019
    1NDC:55443-0600-22 in 1 BOX
    1NDC:55443-0600-11000 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00310/01/2019
    Labeler - Metrex Research, LLC (145963778)
    Registrant - Metrex Research (145963778)
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