Label: HANDY SOLUTIONS HAND SANITIZER- alcohol liquid

  • NDC Code(s): 67751-086-01, 67751-086-02
  • Packager: Navajo Manufacturing Company Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 15, 2024

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  • Active ingredient

    Ethyl Alcohol 70% v/v

  • Purpose

    Antimicrobial

  • Uses

    • A hand sanitizer to help reduce bacteria on the skin
  • Warnings

    Flammable. Keep away from fire or flame.

    For external use only.

    When using this product do not use in or near eyes. In case of contact, rinse eyes thoroughly with water.

    Stop use and ask a doctor if irritation or rash appears and lasts.

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • Put enough product in your palm to cover hands and rub hands together briskly until dry.
    • Children under 6 years of age should be supervised when using this product.
  • Other information

    • Store below 110°F (43°C).
    • May discolor certain fabrics or surfaces.
  • Inactive ingredients

    Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aloe Barbadensis Leaf Juice, Fragrance(Parfum), Glycerin, Maltodextrin, Propylene Glycol, Tocopheryl Acetate, Triethanolamine, Water(Aqua).

  • Questions or comments?

    Call 1-800-525-5097

  • Package Labeling

    Handy Solutions Hand Sanitizer

    Carded Handy Solutions Hand Sanitizer

  • INGREDIENTS AND APPEARANCE
    HANDY SOLUTIONS HAND SANITIZER 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67751-086
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    WATER (UNII: 059QF0KO0R)  
    ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:67751-086-021 in 1 PACKAGE06/30/2023
    159 mL in 1 BOTTLE; Type 0: Not a Combination Product
    2NDC:67751-086-0159 mL in 1 BOTTLE; Type 0: Not a Combination Product06/30/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)06/30/2023
    Labeler - Navajo Manufacturing Company Inc. (091917799)
    Registrant - Navajo Manufacturing Company Inc. (136941411)
    Establishment
    NameAddressID/FEIBusiness Operations
    Nantong Health & Beyond Hygienic Products Inc.421280161manufacture(67751-086)
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