Label: COMPANION HAND SANITIZER- hand sanitizer liquid

  • NDC Code(s): 59051-7100-1, 59051-7100-2, 59051-7100-3
  • Packager: Neogen Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 16, 2024

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  • DRUG FACTS Active ingredients

    Ethyl Alcohol 62%

  • PURPOSE

    Antimicrobial

  • USES

    • For hand sanitizing to decrease disease causing dermal bacteria
    • Recommend for repeated use.
  • WARNINGS

    Flammale.  Keep away from fire or flame.

    For External use only.

    When using this product avoid contact with eyes.  In case of eye contact, flush eyes with water.

    Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours.

  • KEEP OUT OF REACH OF CHILDREN

    If swallowed, get medical help or contact a Poison Control Center right away.

  • DIRECTIONS

    Place 2 pumps of product into your palm.  Rub hands together briskly until dry.  Children under 6 years of age should be supervised when using this product.

    OTHER INFORMATION

    Store below 110°F (43°C).  May discolor certain fabrics or surfaces.

    INACTIVE INGREDIENTS

    Water, DEA C8-18, Glycerin

  • PRINCIPAL DISPLAY PANEL

    COMPANION

    Hand Sanitizer

    • Kills 99.9% of harmful bacteria on contact.
    • Foaming action.

    ​Manufactured For:Neogen Corporation

    944 Nandino Blvd.

    Lexington, KY  40511 USA

    800-477-8201 (USA/Canada) or 859-254-1221  L4849-1216

    Companion Hand Sanitizer

  • INGREDIENTS AND APPEARANCE
    COMPANION HAND SANITIZER 
    hand sanitizer liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59051-7100
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL338.82 g  in 1 L
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PEG-10 ACRYLATE/PERFLUOROHEXYLETHYL ACRYLATE COPOLYMER (UNII: D76Z87928N)  
    2-(PERFLUOROHEXYL)ETHANOL (UNII: G2R5YO5N3V)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:59051-7100-216 in 1 PACKAGE, COMBINATION06/05/201709/05/2025
    1NDC:59051-7100-10.2 L in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
    2NDC:59051-7100-33.78 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/05/201712/16/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)06/05/201709/05/2025
    Labeler - Neogen Corporation (042125879)
    Registrant - Preserve International (117315289)
    Establishment
    NameAddressID/FEIBusiness Operations
    Preserve Inc.808154199manufacture(59051-7100) , api manufacture(59051-7100)
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