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Handi Sani (Vi-Jon)

Available Formats

Dosage Form Package Information Links
LIQUID .073 L in 1 BOTTLE, PLASTIC (11344-484-18) Label Information
LIQUID .059 L in 1 BOTTLE, PLASTIC (11344-484-16) Label Information
LIQUID .089 L in 1 BOTTLE, PLASTIC (11344-484-21) Label Information
LIQUID .236 L in 1 BOTTLE, PLASTIC (11344-484-34) Label Information

Complete Handi Sani Information

  • ACTIVE INGREDIENT

    Active ingredients
    Ethyl Alcohol 62%

    Purpose
    Antiseptic

  • INDICATIONS & USAGE

    Uses to decrease bacteria on the skin that could cause disease
    recommend for repeated use

  • WARNINGS

    Warnings
    For external use only-hands

    Flammable.  Keep away from heat and flame.

    When using this product Keep out of eyes.  In case of contact with eyes, flush thoroughly with water.
    avoid contact with broken skin do not inhale or ingest

    Stop use and ask a doctor if skin irritation develops

    Keep out of reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.

  • DOSAGE & ADMINISTRATION

    Directions wet hands thoroughly with product and allow to dry without wiping for children under 6, use adult supervision
    not recommended for infants

  • STORAGE AND HANDLING

    Other information do not store above 105⁰ F may discolor some fabrics harmful to wood finishes and plastics

  • INACTIVE INGREDIENT

    Inactive ingredients benzophenone-4, blue 1, carbomer, fragrance, glycerin, isopropyl alcohol, isopropyl myristate, propylene glycol, red 33, tocopheryl acetate, water

  • ADVERSE REACTIONS

    Distributed By: Vi-Jon
    8515 Page Ave
    St. Louis, MO 63114

  • PRINCIPAL DISPLAY PANEL

    Handi Sani
    Hand Sanitizer
    Germ-X
    2 FL OZ (59 mL)
    imiage of principal display panel

  • INGREDIENTS AND APPEARANCE
    HANDI SANI 
    alcohol liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:11344-484
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 62 mL  in 100 L
    Inactive Ingredients
    Ingredient Name Strength
    SULISOBENZONE (UNII: 1W6L629B4K)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:11344-484-16 .059 L in 1 BOTTLE, PLASTIC
    2 NDC:11344-484-18 .073 L in 1 BOTTLE, PLASTIC
    3 NDC:11344-484-21 .089 L in 1 BOTTLE, PLASTIC
    4 NDC:11344-484-34 .236 L in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333A 04/02/2012
    Labeler - Vi-Jon (150931459)
    Registrant - Vi-Jon (790752542)
    Establishment
    Name Address ID/FEI Business Operations
    Vi-Jon 088520668 manufacture