Label: EON HAND SANITIZING MIST TM- ethyl alcohol spray

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated January 6, 2021

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  • ACTIVE INGREDIENT

    Ethyl Alcohol 80% v/v

  • PURPOSE

    Antiseptic

  • INDICATIONS & USAGE

    Hand sanitizer to help reduce germs that can potentially cause disease. For use when soap and water are not available

  • WARNINGS

    For external use only. Flammable. Keep away from heat or flame. Do not puncture or incinerate. Contents under pressure.

  • DO NOT USE

    • on children less than 2 months of age
    • on open skin wounds
  • WHEN USING

    keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

  • STOP USE

    if irritation or rash occurs. These may be signs of a serious condition.

  • KEEP OUT OF REACH OF CHILDREN

    If swallowed, get medical help or contact a Poison Control Center.

  • DOSAGE & ADMINISTRATION

    • Place enough product on hands to cover all surfaces. Rub hands together until dry.
    • Supervise children under 6 years of age when using hit produce to avoid swallowing.
  • OTHER SAFETY INFORMATION

    • Store between 15-30 oC (59-86 oF)
    • Avoid freezing. Do not expose to heat above 40 oC (104 oF)
  • INACTIVE INGREDIENT

    Glycerin, Hydrogen Peroxide, Purified Water

  • EON Hand Sanitizing Mist TM

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  • INGREDIENTS AND APPEARANCE
    EON HAND SANITIZING MIST TM 
    ethyl alcohol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73787-135
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL80 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    HYDROGEN PEROXIDE (UNII: BBX060AN9V)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73787-135-0159.14 mL in 1 BOTTLE; Type 0: Not a Combination Product09/10/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E09/10/2020
    Labeler - FGD, LLC (111927555)
    Establishment
    NameAddressID/FEIBusiness Operations
    Goodwin Co.806987483manufacture(73787-135)
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