Label: DR.S CLEAN HAND SANITIZER- 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 May 5, 2020

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  • Drug Facts

  • Active ingredients

    Ethyl Alcohol 70.0%

  • Purpose

    ANTISEPTIC

  • Uses

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

  • 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 ifirritation or redness develops.

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

  • Directions

    • Wet hands thoroughly with product and allow to dry without wiping.

    • For children under 6, use only under adult supervision.

  • Inactive Ingredients

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

  • Questions?

    310.537.7662 or visit http://www.megaexhibit.com

  • SPL UNCLASSIFIED SECTION

    HAND GEL

    Simply KILL 99.9% Germ

    Leaves Hands Feeling Soft

    ADVANCED

    (ethanol) contented 

    ERF

    12854 E. Florence Ave. Santa Fe Springs, CA 90670

  • Packaging

    untitled

  • INGREDIENTS AND APPEARANCE
    DR.S CLEAN HAND SANITIZER 
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76724-001
    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:76724-001-05500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/04/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A05/04/2020
    Labeler - Erf Exhibit Inc (099461452)
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