Label: CASEYS ANTIMICROBIAL HAND SANITIZER- ethyl alcohol gel

  • NDC Code(s): 67751-071-01, 67751-071-02
  • Packager: Navajo Manufacturing Company Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 29, 2024

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  • ACTIVE INGREDIENT

    Active ingredient

    Ethyl Alcohol, 70% v/v

  • PURPOSE

    Purpose  Antimicrobial

  • INDICATIONS & USAGE

    Uses

    • for hand sanitizing to decrease bacteria on the skin
    • recommended for repeated use
  • WARNINGS

    Warnings

    For external use only.

    Flammable, keep away from heat or flame.

  • WHEN USING

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

  • STOP USE

    Stop use and ask a doctor if irritation or redness develop and persist for more than 72 hours

  • KEEP OUT OF REACH OF CHILDREN

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

  • DOSAGE & ADMINISTRATION

    Directions 

    • wet hands thoroughly with product
    • briskly rub hands together until dry
    • supervise children under 6 years in the use of this product
  • STORAGE AND HANDLING

    Other information

    • store at room temperature
    • may discolor certain fabrics
  • INACTIVE INGREDIENT

    Inactive ingredients

    Water (aqua), Propylene Glycol, Glycerin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Fragrance, Triethanoamine, Aloe Barbadensis Leaf Juice, Maltodextrin, Tocopherylacetate

  • PRINCIPAL DISPLAY PANEL

    image description

  • INGREDIENTS AND APPEARANCE
    CASEYS ANTIMICROBIAL HAND SANITIZER 
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67751-071
    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
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)  
    TOCOPHERYL GLUCOSIDE (UNII: 9CKD1JE38R)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    ALOE ARBORESCENS LEAF (UNII: 09TD8L5SQV)  
    TRICLOSAN (UNII: 4NM5039Y5X)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorAPPLE (candy apple) Imprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:67751-071-0159 mL in 1 BOTTLE; Type 0: Not a Combination Product04/29/2024
    2NDC:67751-071-02236 mL in 1 BOTTLE; Type 0: Not a Combination Product04/29/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00504/29/2024
    Labeler - Navajo Manufacturing Company Inc. (091917799)
    Establishment
    NameAddressID/FEIBusiness Operations
    Nantong Health & Beyond Hygienic Products Inc.421280161manufacture(67751-071)
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