Label: DR.S CLEAN HAND- 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 April 18, 2020

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  • ACTIVE INGREDIENT

    Active ingredients: Ethyl Alcohol 70.0%

  • INACTIVE INGREDIENT

    Inactive ingredients:

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

  • PURPOSE

    Purpose: ANTISEPTIC

  • WARNINGS

    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

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

  • Directions

    Directions:

    Wet hands thoroughly with product and allow to dry without wiping

    For children under 6, use only under adult supervision.

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    Image of bottle

  • INGREDIENTS AND APPEARANCE
    DR.S CLEAN HAND 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55526-0011
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 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:55526-0011-1500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product04/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E04/01/2020
    Labeler - EQMAXON Corp (557821534)
    Registrant - EQMAXON Corp (557821534)
    Establishment
    NameAddressID/FEIBusiness Operations
    EQMAXON Corp557821534manufacture(55526-0011)
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