Label: DR.S CLEAN ADVANCED HAND- 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 July 27, 2020

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  • ACTIVE INGREDIENT

    Ethyl Alcohol 70.0%

  • INACTIVE INGREDIENTS

    Purified Water, Aloe Extract, Glycerin, Sodium Hyaluronate, Carbomer, Butylene Glycol, Triethanolamine, Flavoring

  • PURPOSE

    ANTISEPTIC

  • WARNINGS

    Flammable. Keep away from fire and flames. For external use only.


    When using this product • Do not get into eyes. • If contact occurs, rinse eyes thoroughly with water.


    Stop use and ask a doctor if irritation or redness develops.


    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

  • 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

  • Uses

    for hand-washing to decrease bacteria on the skin, only when water is not available

  • Directions

    Wet hands thoroughly with product and allow to dry without wiping

    For children under 6, use only under adult supervision.

  • Questions

    Questions?

    +82-31-429-8582 or visit http://www.eqmaxon.com

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    Image of bottle

  • INGREDIENTS AND APPEARANCE
    DR.S CLEAN ADVANCED HAND 
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55526-0016
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL42 mL  in 60 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    ALOE (UNII: V5VD430YW9)  
    Glycerin (UNII: PDC6A3C0OX)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    Butylene Glycol (UNII: 3XUS85K0RA)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:55526-0016-160 mL in 1 BOTTLE; Type 0: Not a Combination Product07/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E07/01/2020
    Labeler - EQMAXON Corp (557821534)
    Registrant - EQMAXON Corp (557821534)
    Establishment
    NameAddressID/FEIBusiness Operations
    EQMAXON Corp557821534manufacture(55526-0016)
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