Label: CLEAN ON HAND SANITIZER PLUS- alcohol gel

  • Category: HUMAN OTC DRUG LABEL

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 June 10, 2020

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  • ACTIVE INGREDIENT

    Alcohol 70.0% w/w

  • INACTIVE INGREDIENTS

    Water, Carbomer, Triethanolamine, Glycerin, Propylene Glycol, Panthenol, Dipotassium Glycyrrhizate, Aloe Barbadensis Leaf Juice, Sodium Hyaluronate, Tocopheryl Acetate, Rosemary Extract

  • PURPOSE

    SANITIZER

  • WARNINGS

    For external use only. Flammable. Keep away from heat or flame

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    Do not use
    • in children less than 2 months of age
    • on open skin wounds
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    When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
    --------------------------------------------------------------------------------------------------------
    Stop use and ask a doctor 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 right away.

  • Uses

    Hand sanitizer to help reduce bacteria on the skin that could cause disease.

    Recommended for repeated use.

  • Directions

    Take an appropriate amount on your hands and rub thoroughly to dry.

    Children under 6 years of age should be supervised when using this product.

  • Other Information

    • Store between 15-30℃ (59-86℉)

    • Avoid freezing and excessive heat above 40℃ (104℉)

  • Package Label: CLEAN ON HAND SANITIZER GEL PLUS 1gal

    Image of bottle

  • Package Label: CLEAN ON HAND SANITIZER GEL PLUS 5L

    Image of bottle

  • INGREDIENTS AND APPEARANCE
    CLEAN ON HAND SANITIZER PLUS 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74522-030
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Alcohol (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) Alcohol0.7 kg  in 1 L
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    Glycerin (UNII: PDC6A3C0OX)  
    Propylene Glycol (UNII: 6DC9Q167V3)  
    Panthenol (UNII: WV9CM0O67Z)  
    GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:74522-030-013.78 L in 1 BOTTLE; Type 0: Not a Combination Product06/01/2020
    2NDC:74522-030-025 L in 1 BOTTLE; Type 0: Not a Combination Product06/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E06/01/2020
    Labeler - Caolion Cosmetics Co., Ltd. (557792513)
    Registrant - Caolion Cosmetics Co., Ltd. (557792513)
    Establishment
    NameAddressID/FEIBusiness Operations
    KOREA COSPACK CO.,LTD.689059789manufacture(74522-030)