Label: ZEP HANDSTAND INSTANT HAND SANITIZER- ethyl alcohol liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 18, 2024

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  • Active Ingredient

    Ethyl Alcohol 62%

  • Purpose

    Antiseptic Agent

  • Uses

    Hand sanitizer to help reduce bacteria on the skin that could cause disease. Recommended for repeated use.

  • Warnings

    Flammable. Keep away from heat or flame.

    For external use only.

  • Do not use

    Do not use in the eyes. In case of contact, rinse thoroughly.

  • Stop use and ask a doctor

    Stop use and ask a doctor if irritation and redness appears and lasts.

  • Keep out of reach of children

    Keep out of reach of children. If swallowed, contact a physician or poison control center.

  • Directions

    • To decrease bacteria on skin, apply a small amount to palm. Briskly rub, covering hands with product until dry.
    • Children should be supervised when using this product.
  • Inactive Ingredients

    Water, Glycerin, Propylene Glycol, Isopropyl Myristate, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate (Vitamin E), Carbomer, Aminomethyl Propanol

  • QUESTIONS

    www.zep.com

  • PRINCIPAL DISPLAY PANEL

    906_0906

  • INGREDIENTS AND APPEARANCE
    ZEP HANDSTAND INSTANT HAND SANITIZER 
    ethyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66949-906
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:66949-906-019600 mL in 1 CASE; Type 0: Not a Combination Product09/05/1997
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)09/05/1997
    Labeler - Zep Inc. (030471374)
    Establishment
    NameAddressID/FEIBusiness Operations
    Kutol Products Company004236139manufacture(66949-906)
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