Label: BEN E.KEITH HAND CLEANER- ethyl alcohol gel

  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated March 1, 2024

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  • Active Ingredient

    Ethyl Alcohol 62% v/v

  • Purpose

    Antibacterial Agent

  • Uses

    For handwashing to decrease bacteria on skin.

  • Warnings

    For external use only

    Flammable Keep away from heat or flame.

    Do not use in Eyes

    Stop use if redness and irritation develop.  If condition persists for more than 72 hours, consult a physician.

    Stop use if redness and irritation develop. If condition persists for more than 72 hours, consult a physician.

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

  • Directions

    To decrease bacterial on skin, apply a small amount to palm.  Briskly rub, covering hands withproduct until dry.

  • Inactive ingredients

    Water, glycerin, propylene glycol, isopropyl myristate, aloe barbadensis leaf, tocopheryl acetate (Vitamin E), Carbomer, Aminomethyl propanol.

  • Principal Display Panel and representative label

    DELIVERING QUALITY SINCE 1906

    BEN E. 

    KEITH

    CO.

    FOODSERVICE DISTRIBUTORS

    GEL INSTANT HAND SANITIZER

    Net Contents: 8 Fl. Oz. (237 mL)

    Distributed by:

    BEN E. KEITH FOODS Fort Worth, TX 76101

    MADE IN USA

    representative label

  • INGREDIENTS AND APPEARANCE
    BEN E.KEITH  HAND CLEANER
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50980-056
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    CARBOMER 1342 (UNII: 809Y72KV36)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:50980-056-19237 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product01/02/2009
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)01/02/2009
    Labeler - Ben E. Keith (007929748)
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