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Hand Sanitizer (McKesson)

Available Formats

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GEL .236 L in 1 BOTTLE, PLASTIC (49348-982-37) Label Information

Complete Hand Sanitizer Information

  • ACTIVE INGREDIENT

    Active Ingredient
    Ethyl Alcohol 65%

    Purpose
    Antiseptic

  • INDICATIONS & USAGE

    Uses to decrease bacteria on the skin that could cause disease recommended 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.
    do not inhale or ingest avoid contact with broken skin

    Stop use and ask a doctor if skin irritation develops.

    Keep out of reach of children.  In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

  • DOSAGE & ADMINISTRATION

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

  • OTHER SAFETY INFORMATION

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

  • INACTIVE INGREDIENT

    Inactive ingredients aloe barbadensis leaf juice, benzophenone-4, blue 1, carbomer, fragrance, glycerin, isopropyl myristate, propylene glycol, tocopheryl acetate, water, yellow 5.

  • SPL UNCLASSIFIED SECTION

    Effective at eliminating over 99.99% of many common harmful germs and bacteria in as little as 15 seconds.
    Made in USA with US and foreign components.
    Not manufactured or distributed by Johnson and Johnson, the owner and distributor of Purell Hand Sanitizer

  • PRINCIPAL DISPLAY PANEL

    Sunmark
    Compare to
    Purell
    NDC 49348-982-37
    Hand
    Sanitizer
    Kills germs
    without water
    WITH ALOE
    8 FL OZ (236 mL)
    image of principal display panel

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER 
    ethyl alcohol gel
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:49348-982
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 65.0 mL  in 100 L
    Inactive Ingredients
    Ingredient Name Strength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    SULISOBENZONE (UNII: 1W6L629B4K)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    CARBOMER INTERPOLYMER TYPE A (55000 MPA.S) (UNII: 59TL3WG5CO)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    WATER (UNII: 059QF0KO0R)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:49348-982-37 .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 08/02/2011
    Labeler - McKesson (177667227)
    Registrant - Vi-Jon (088520668)
    Establishment
    Name Address ID/FEI Business Operations
    Vi-Jon 088520668 manufacture