Label: MED X FRONTLINE ADVANCED HAND SANITIZER WITH MOISTURIZERS AND VITAMIN E- alcohol gel

  • NDC Code(s): 74934-073-01, 74934-073-02, 74934-073-03
  • Packager: Zhejiang iColor Biotech Co., Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 24, 2024

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  • Drug Facts

  • Active Ingredients

    Ethyl alcohol 75% v/v

    Purpose

    Antiseptic

  • Uses

    • For hand washing to help reduce bacteria that potentially can cause disease. Recommended for repeated use. For use when soap and water are not available.
  • Warnings

    For external use only
    Flammable. Keep away from heat or flame

    When using this product

    do not use in or near eyes,ears and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

    Stop use and ask a doctor 

    if irritation or rash appears on the skin.

    Keep out of reach of children.

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

  • Directions

    • Place enough product on hands to cover all surfaces. Rub hands together until dry.
    • Children under 6 years of age should be supervised by adult when applying this product.
    • Do not use on children less than 2 months of age or on open skin wounds.
  • Other information

    • Store between 15-30 oC (59-86°F)
    • Avoid freezing and excessive heat above 40°C (104°F)
    • May discolor some fabrics or surtaces
  • Inactive ingredients

    Water, Glycerin, Squalane, Panthenol, Inulin, Sodium Hyaluronate, Fructose,Tocopheryl Acetate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyi Propanol.

  • Package Labeling(236 ml)

    236 ml

  • Package Labeling(3.8 L)

    Bottle 3.8

  • Package Labeling(500 ml)

    Bottle 500 ml.jpg

  • INGREDIENTS AND APPEARANCE
    MED X FRONTLINE ADVANCED HAND SANITIZER WITH MOISTURIZERS AND VITAMIN E 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74934-073
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.75 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SQUALANE (UNII: GW89575KF9)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    INULIN (UNII: JOS53KRJ01)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    FRUCTOSE (UNII: 6YSS42VSEV)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:74934-073-01236 mL in 1 BOTTLE; Type 0: Not a Combination Product12/05/202001/31/2026
    2NDC:74934-073-023800 mL in 1 BOTTLE; Type 0: Not a Combination Product12/05/202001/31/2026
    3NDC:74934-073-03500 mL in 1 BOTTLE; Type 0: Not a Combination Product12/05/202001/31/2026
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)12/05/202001/31/2026
    Labeler - Zhejiang iColor Biotech Co., Ltd (554528308)
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