Label: HAND SANITIZER- alcohol cloth

  • 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 November 18, 2020

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  • Active Ingredient

    Ethyl Alcohol (65%)

  • Purpose

    Antimicrobial

  • Uses

    • Recommended for use on skin to sanitize and help minimize exposure to bacteria.

    • Use multiple wipes daily as needed.

  • Warnings

    • For external use only. Flammable: Keep away from fire or flame. • When using this product do not use on damaged or broken skin. • Do not use in or near eyes and mouth.
    If contact occurs, flush thoroughly with water. • Stop use and consult physician if irritation or rash occurs or 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

    • Remove wipe from pouch

    • Thoroughly cleanse hands with wipe

    • Allow hands to dry without wiping

  • Other information

    • Store in a cool, dry place.

  • Inactive ingredients

    water, glycerin, aloe barbadensis leaf extract, althaea officinalis root extract, chamomilla recutita (matricaria) flower extract, cucumis sativus (cucumber) fruit extract, avena sativa (oat) kernel extract, camellia sinensis leaf extract, lavandula angustifolia (lavender) oil

  • Label

    CLEAN. DISINFECT & PROTECT.

    SANITIZING HAND WIPES

    WITH SKIN NOURISHING BOTANICALS

    KILLS 99.99% OF GERMS

    PARABEN-FREE

    TRICLOSAN-FREE

    NO BENZALKONIUM ADDED

    30 CT. WIPES

    Formulated in the U.S.A. for:

    YOUNGEVITY

    2400 Boswell Road

    Chula Vista, CA 91914

    www.youngevity.com

    (800) 982-3189 LABEL

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER 
    alcohol cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80986-100
    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
    GLYCERIN (UNII: PDC6A3C0OX)  
    LAVENDER OIL (UNII: ZBP1YXW0H8)  
    WATER (UNII: 059QF0KO0R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CUCUMBER (UNII: YY7C30VXJT)  
    ALTHAEA OFFICINALIS ROOT (UNII: TRW2FUF47H)  
    OAT (UNII: Z6J799EAJK)  
    GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
    CHAMOMILE (UNII: FGL3685T2X)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:80986-100-301 mL in 1 POUCH; Type 0: Not a Combination Product11/30/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E11/30/2020
    Labeler - Youngevity International Inc. (078524610)
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