Label: MUSE HEALTH HAND SANITIZER- ethyl alcohol gel

  • 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 April 26, 2022

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  • ACTIVE INGREDIENT

    Ethyl Alocohol 62% by wt.

  • PURPOSE

    Antiseptic

  • Uses

    To decrease bacteria on the skin that could cause disease.

    Recommended for repeated use.

  • WARNINGS

    For external use only: hands

    Flammable, keep away from fire or flame.

    When using this product

    Keep out of eyes.

    In case of contact with eyes, flush thoroughly with water.

    Avoid contact with broken skin.

    Do not inhale or ingest.

    Stop use and ask a doctor

    Irritation and redness develop

    Condition persists for more than 72 hours

  • KEEP OUT OF REACH OF CHILDREN

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

  • Directions

    Wet hands thoroughly with product and allow to dry without wiping.

    For children under 6, use only under adult supervision.

    Not recommended for infants.

  • Other Information

    Do not store above 105°

    May discolor some fabrics

    Harmful to wood finishes and plastics

  • INACTIVE INGREDIENT

    Water (Aqua), Glycerin, Tocopheryl Acetate, Isopropyl Palmitate, Acrylates Copolymer, Aminomethyl Propranolol, Parfum

  • Questions?

    feedback@musehealth.com

  • Principle Display Panel

    Product Labeling

  • INGREDIENTS AND APPEARANCE
    MUSE HEALTH HAND SANITIZER 
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71683-011
    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
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    ACRYLATES CROSSPOLYMER-6 (UNII: 4GXD0Q3OS3)  
    AMINOMETHYL PROPANEDIOL (UNII: CZ7BU4QZJZ)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71683-011-01240 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/06/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A08/06/2020
    Labeler - CC Wellness (067692292)
    Establishment
    NameAddressID/FEIBusiness Operations
    CC Wellness, LLC067692292manufacture(71683-011)
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