Label: WAXMAN KLEEN FREAK HAND SANITIZER- alcohol gel

  • NDC Code(s): 66902-750-12
  • Packager: Natural Essentials, Inc.
  • 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 September 1, 2020

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  • Active Ingredients

    Ethyl Alcohol 70%

  • Purpose

    Antiseptic

  • Uses

    For handwashing to decrease bacteria on the skin

  • Warnings

    Flammable. Keep away from fire or flame

    For external use only

    When using this product

    Do not use in eyes. In case of contact with eyes, rinse with water

    Stop use and ask a doctor if

    irritation and redness develop and persist

    Keep out of reach of children

    If swallowed, get medical help promptly

  • Directions

    Wet hands thoroughly with product and allow to dry without wiping. Children under 6 years of age should be supervised when using this product.

  • Other information

    May discolor certain fabrics. Store under 105 F

  • Inactive Ingredients

    Acrylates/Vinyl Isodecanoate Crosspolymer, Aloe Barbadensis Leaf, PEG-6, PEG-12 Dimethicone, Water

    May contain fragrance

  • Principal Display Panel – 1 Gallon Bottle Label

    Kills
    99.9% of
    Germs

    waxman

    kleen
    freak™
    hand sanitizer

    Contains 70% alcohol
    to kill common germs

    1 Gallon

    Principal Display Panel – 1 Gallon Bottle Label
  • INGREDIENTS AND APPEARANCE
    WAXMAN KLEEN FREAK HAND SANITIZER 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66902-750
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M) Alcohol0.70 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER (10000 MPA.S NEUTRALIZED AT 0.5%) (UNII: 2N8MDB79NA)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ)  
    PEG-12 DIMETHICONE (300 CST) (UNII: ZEL54N6W95)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:66902-750-123785 mL in 1 JUG; Type 0: Not a Combination Product09/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A09/01/2020
    Labeler - Natural Essentials, Inc. (947484713)
    Establishment
    NameAddressID/FEIBusiness Operations
    NATURAL ESSENTIALS, INC.947484713MANUFACTURE(66902-750)
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