Label: JTD ADVANCED HAND SANITIZER WITH MOISTURIZERS AND VITAMIN E- alcohol gel

  • NDC Code(s): 77595-004-01, 77595-004-02
  • Packager: J-Tech Digital, INC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 24, 2024

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  • Drug Facts

  • Active Ingredient

    Ethyl Alcohol 70% 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 below 110°F(43°C).
    • May discolor certain fabrics or surfaces.
  • Inactive ingredients

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

  • Bottle Package Labeling:

    Bottle2

  • Tube Package Labeling:

    Tube Label

  • INGREDIENTS AND APPEARANCE
    JTD ADVANCED HAND SANITIZER WITH MOISTURIZERS AND VITAMIN E 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:77595-004
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.7 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:77595-004-0260 mL in 1 BOTTLE; Type 0: Not a Combination Product05/10/202001/31/2026
    2NDC:77595-004-0160 mL in 1 TUBE; Type 0: Not a Combination Product05/10/202001/31/2026
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)05/10/202001/31/2026
    Labeler - J-Tech Digital, INC (031859844)
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