Label: STUVZ HAND SANITIZER- alcohol liquid

  • 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 October 27, 2020

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  • Drug Facts

  • Active Ingredient

    Ethyl Alcohol 62%

  • Purpose

    Antiseptic

  • Uses

    • Hand Sanitizer to help reduce bacteria that potentially cause disease.
    • For use when soap and water are not available.
  • Warnings

    Flammable. Keep away from fire or flame.

    For external use only.

  • WHEN USING

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

  • STOP USE

    Stop use and ask a doctor if irritation or rash occurs.

  • 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.

  • DO NOT USE

    Do Not Use

    • In children less than 2 months of age.
    • On open skin wounds
  • Directions

    • Place enough product in your palm to thoroughly cover your hands.
    • Rub hands briskly until they are fully dry.
  • Other Information

    • Store between 15-30°C (59-86°F).
    • Avoid freezing and excessive heat above 40°C (104°F).
  • Inactive Ingredients

    Water, hydrolized jojoba esters, glycerin, PEG-10 dimethicone, sodium hyaluronate, lavandula hybrida.

  • PRINCIPAL DISPLAY PANEL

    Stuvz Hand Sanitizer

    With Hyaluronic Acid

    5.7 FL. OZ/168 ML Label

  • INGREDIENTS AND APPEARANCE
    STUVZ HAND SANITIZER 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79283-002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.62 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    WATER (UNII: 059QF0KO0R)  
    POLYETHYLENE GLYCOL 500 (UNII: 761NX2Q08Y)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    JOJOBA OIL, RANDOMIZED (UNII: 7F0EV20QYL)  
    LAVANDIN OIL (UNII: 9RES347CKG)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79283-002-01168 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product10/27/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E10/27/2020
    Labeler - MR. HAND, LLC (117563109)
    Establishment
    NameAddressID/FEIBusiness Operations
    Pure Source, LLC080354456manufacture(79283-002)
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