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HAND SANITIZING (GANZ U.S.A., LLC)

Available Formats

Dosage Form Package Information Links
GEL 232 mL in 1 BOTTLE, PUMP (75862-001-01) Label Information
GEL 59 mL in 1 BOTTLE (75862-001-02) Label Information

Complete HAND SANITIZING Information

  • SPL UNCLASSIFIED SECTION

    Drug Facts


  • Active ingredient

    Alcohol 62%


  • Purpose

    Antiseptic


  • Uses

    To decrease bacteria on hands.


  • Warnings

    For external use only.

    Flammable, keep away from fire or 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. In case of accidental ingestion, seek professional assistance or contact Poison Control Center immediately.


  • Directions

    Wet hands thoroughly with product and allow to dry without wiping.


  • Other information

    • Do not store above 105°F.
    • May discolor some fabrics.
    • Harmful to wood finishes and plastics.
    • You may report a serious adverse reaction to this product to: Ganz U.S.A., LLC #043, 60 Industrial Parkway, Cheektowaga, New York, 14227-9903

  • Inactive ingredients

    Water, Fragrance, Glycerin, Triethanolamine, PEG-7 Glyceryl Cocoate, Hydrolyzed Jojoba Esters, Chamomilla Recutita (Matricaria) Flower Extract, Salvia Officinalis (Sage) Leaf Extract, Urtica Dioica (Nettle) Extract, Rosmarinus Officinalis (Rosemary) Leaf Extract, Aloe Barbadensis Leaf Extract, Aloe Barbadensis Leaf Juice, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Blue 1, Yellow 5.


  • PRINCIPAL DISPLAY PANEL - 232 mL Bottle Label

    time&againâ„¢

    HAND SANITIZING GEL

    Formulated with Glycerin,
    Aloe and Jojoba to Moisturize.

    Kills harmful bacteria and germs.

    GREEN APPLE

    232 mL 7.8 fl. OZ.

    PRINCIPAL DISPLAY PANEL - 232 mL Bottle Label

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZING   GREEN APPLE
    alcohol gel
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:75862-001
    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 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L)  
    GLYCERYL COCOATE (UNII: WVK1CT5994)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    JOJOBA OIL (UNII: 724GKU717M)  
    CHAMAEMELUM NOBILE FLOWER (UNII: O2T154T6OG)  
    SAGE (UNII: 065C5D077J)  
    URTICA DIOICA LEAF (UNII: X6M0DRN46Q)  
    ROSEMARY (UNII: IJ67X351P9)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:75862-001-01 232 mL in 1 BOTTLE, PUMP
    2 NDC:75862-001-02 59 mL in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC MONOGRAPH NOT FINAL part333E 01/01/2011
    Labeler - GANZ U.S.A., LLC (798785242)