Label: COMPANION- companion antibacterial hand soap liquid

  • NDC Code(s): 60648-7200-1, 60648-7200-2
  • Packager: Preserve International
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 16, 2024

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  • DRUG FACTS Active ingredients

    Benzalkonium Chloride 0.13%....................Antibacterial

  • PURPOSE

    Antimicrobial

  • USES

    For hand washing to minimize bacteria on the skin.

  • WARNINGS

    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.

  • KEEP OUT OF REACH OF CHILDREN

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

  • DIRECTIONS

    • Pump foam into dry hands.
    • Lather with water for atleast 20 seconds.
    • Rinse and pat dry.

    OTHER INFORMATION

    Store below 110°F (43°C). 

    INACTIVE INGREDIENTS

    Water, Xanthan Gum, Glycerin, Sodium Lauryl Eather Sulfate, Alkylpolyglycoside, Cocamidopropyl Betaine, Citric Acid, Sodium Citrate, Tetrasodium Ethylenediamine Tetraacetate, Sodium Benzoate, Waterfall Mist, Blue #1, Yellow #5.

  • PRINCIPAL DISPLAY PANEL

    COMPANION

    Foaming Antibacterial Hand Soap

    • Kills 99.9% of common bacteria
    • Moisturizing Formula
    • Light Fresh Scent

    NET CONTENTS: 16.9 oz. (750 ml)

    Item No.: 4900912/6

    ​Manufactured By:

    Preserve International, a wholly-owned subsidiary of Neogen ®

    944 Nandino Blvd. Lexington, KY 40511 USA

    800-477-8201 (USA/Canada) or 859-254-1221 L7018-0920

    CompanionAntibacterial Hand Soap

  • INGREDIENTS AND APPEARANCE
    COMPANION 
    companion antibacterial hand soap liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:60648-7200
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE2.9 mg  in 1 L
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    DECYL GLUCOSIDE (UNII: Z17H97EA6Y)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:60648-7200-10.75 L in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product11/04/202009/05/2025
    2NDC:60648-7200-23.78 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/04/202009/05/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)11/04/202009/05/2025
    Labeler - Preserve International (808154199)
    Registrant - Preserve International (808154199)
    Establishment
    NameAddressID/FEIBusiness Operations
    Preserve International808154199manufacture(60648-7200) , api manufacture(60648-7200)
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