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Hand-E XL (ABC Compounding Co., Inc.)

Available Formats

Dosage Form Package Information Links
GEL 473 mL in 1 BOTTLE, PLASTIC (62257-606-30) Label Information
GEL 208200 mL in 1 DRUM (62257-606-55) Label Information
GEL 149 mL in 1 BOTTLE, PLASTIC (62257-606-28) Label Information
GEL 540 mL in 1 BOTTLE, PLASTIC (62257-606-05) Label Information
GEL 800 mL in 1 BAG (62257-606-13) Label Information
GEL 1000 mL in 1 CARTRIDGE (62257-606-10) Label Information
GEL 118 mL in 1 BOTTLE, PLASTIC (62257-606-24) Label Information
GEL 2000 mL in 1 CARTRIDGE (62257-606-09) Label Information
GEL 1000 mL in 1 BAG (62257-606-12) Label Information
GEL 1200 mL in 1 CARTRIDGE (62257-606-01) Label Information
GEL 350 mL in 1 CARTRIDGE (62257-606-03) Label Information
GEL 1 BAG in 1 BOX (62257-606-08) > 1000 mL in 1 BAG Label Information
GEL 532 mL in 1 BOTTLE, PLASTIC (62257-606-17) Label Information
GEL 946 mL in 1 BOTTLE, PLASTIC (62257-606-15) Label Information
GEL 1000 mL in 1 BOTTLE, PLASTIC (62257-606-11) Label Information
GEL 700 mL in 1 BAG (62257-606-07) Label Information
GEL 3785 mL in 1 BOTTLE, PLASTIC (62257-606-14) Label Information
GEL 800 mL in 1 CARTRIDGE (62257-606-27) Label Information
GEL 1 BAG in 1 BOX (62257-606-06) > 800 mL in 1 BAG Label Information

Complete Hand-E XL Information

  • Drug Facts Box OTC-Active Ingredient Section

    Ethyl Alcohol 62%


  • Drug Facts Box OTC-Purpose Section

    Antiseptic


  • Drug Facts Box OTC-Indications & Usage Section

    for hand-washing to decrease bacteria on the skin, only when water is not available


  • Drug Facts Box OTC-Warnings Section

    FLAMMABLE, keep away from fire and flames

    For external use only


  • Drug Facts Box OTC-When Using Section

    do not get into eyes

    if contact occurs, rinse eyes thoroughly with water


  • Drug Facts Box OTC-Stop Use Section

    irritation and redness develop


  • Drug Facts Box OTC-Keep Out of Reach of Children Section

    if swallowed, get medical help or contact a Poison Control Center right away


  • Drug Facts Box OTC-Dosage & Administration Section

    wet hands thoroughly with product and allow to dry without wiping


  • Drug Facts Box OTC-Inactive Ingredient Section

    water, diisopropylamine, carbomer, propylene glycol, tocopheryl acetate, aloe barbadensis


  • Hand-E XL 6605 16 oz

    660516PTEK.jpg  Hand-E XL  16 oz  image of bottle label


  • INGREDIENTS AND APPEARANCE
    HAND-E XL 
    alcohol gel
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:62257-606
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.7 mL  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    CARBOMER 934 (UNII: Z135WT9208)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)  
    DIISOPROPYLAMINE (UNII: BR9JLI40NO)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:62257-606-06 1 in 1 BOX
    1 800 mL in 1 BAG
    2 NDC:62257-606-17 532 mL in 1 BOTTLE, PLASTIC
    3 NDC:62257-606-24 118 mL in 1 BOTTLE, PLASTIC
    4 NDC:62257-606-01 1200 mL in 1 CARTRIDGE
    5 NDC:62257-606-03 350 mL in 1 CARTRIDGE
    6 NDC:62257-606-05 540 mL in 1 BOTTLE, PLASTIC
    7 NDC:62257-606-07 700 mL in 1 BAG
    8 NDC:62257-606-09 2000 mL in 1 CARTRIDGE
    9 NDC:62257-606-10 1000 mL in 1 CARTRIDGE
    10 NDC:62257-606-11 1000 mL in 1 BOTTLE, PLASTIC
    11 NDC:62257-606-12 1000 mL in 1 BAG
    12 NDC:62257-606-13 800 mL in 1 BAG
    13 NDC:62257-606-14 3785 mL in 1 BOTTLE, PLASTIC
    14 NDC:62257-606-15 946 mL in 1 BOTTLE, PLASTIC
    15 NDC:62257-606-28 149 mL in 1 BOTTLE, PLASTIC
    16 NDC:62257-606-27 800 mL in 1 CARTRIDGE
    17 NDC:62257-606-55 208200 mL in 1 DRUM
    18 NDC:62257-606-08 1 in 1 BOX
    18 1000 mL in 1 BAG
    19 NDC:62257-606-30 473 mL in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333E 04/01/2005
    Labeler - ABC Compounding Co., Inc. (003284353)
    Establishment
    Name Address ID/FEI Business Operations
    ABC Compounding Co., Inc. 003284353 manufacture