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
  • 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 24, 2023

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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 Product11/04/2020
    2NDC:60648-7200-23.78 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/04/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E11/04/2020
    Labeler - Preserve International (808154199)
    Registrant - Preserve International (808154199)
    Establishment
    NameAddressID/FEIBusiness Operations
    Preserve International808154199manufacture(60648-7200) , api manufacture(60648-7200)
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