Label: HERO WIPES EMS- alcohol hand sanitizer wipes cloth

  • NDC Code(s): 64709-256-10
  • Packager: Diamond Wipes International, Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 4, 2023

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  • Active Ingredients (in each wipe)

    Ethyl Alcohol 65% v/v

  • Purpose

    Antimicrobial

  • Uses

    for hand sanitizing to decrease bacteria on skin

    safe for repeated use

  • Warnings

    For external use only.

    Flammable, keep away from fire or flame.

    When using this product avoid contact with eyes. If in eyes, flush thoroughly with water.

  • 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.

  • Directions

    • to use, open cap and pull out wipe
    • wipe hands thoroughly with product and allow to dry
    • throw used wipe in trash, do not flush
  • Inactive ingredients

    Aloe Barbadensis Leaf Juice, Citric Acid, Potassium Sorbate, Sodium Benzoate, Tocopheryl Acetate, Water

  • Label info

    Front panel

    A PROUD AMERICAN PRODUCT ASSEMBLED IN USA

    hero wipes EMA

    EWG VRETIFIED FOR YOUR HEALTH EWG.ORG

    REDUCE INFECTION RISK

    Kills 99.9% of bacterial pathogens to reduce infection risk

    Strong, stretchable towel

    Back panel

    Drug facts box

    hero wipes EMS

    Hero Wipes EMS is designed for emergency medical service and healthcare professionals. Complies with OSHA's Bloodborne Pathogens standard requirements. Also meets CDC's guideline for hand hyiene in healthcare settings.

    Made in the USA with domestic and goreign components.

    Manufactured by Diamond Wipes International, Chino, CA91710

    www.myherowipes.com | team@myherowipes.com

    Diamond Wipes International

    Not for individual resale

    fast acting

    broad spectrum

    LAB TESTED

    label

  • INGREDIENTS AND APPEARANCE
    HERO WIPES EMS 
    alcohol hand sanitizer wipes cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64709-256
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL65 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    WATER (UNII: 059QF0KO0R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:64709-256-101 mL in 1 PACKET; Type 0: Not a Combination Product01/01/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)01/01/2022
    Labeler - Diamond Wipes International, Inc (161104729)
    Registrant - Diamond Wipes International, Inc (161104729)
    Establishment
    NameAddressID/FEIBusiness Operations
    Diamond Wipes International, Inc161104729manufacture(64709-256)
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