Label: VETONE- vetone sanctuary foaming antibacterial hand soap liquid

  • NDC Code(s): 13985-763-01, 13985-763-16
  • Packager: MWI/VETONE
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 16, 2024

If you are a consumer or patient please visit this version.

View All Sections
  • 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

    VetOne Sanctuary
    Foaming Antibacterial Hand Soap

    • Kills 99.9% of Common Bacteria
    • Moisturizing Formula
    • Light Fresh Scent

    VetOne Sanctuary Hand Soap - 16.9 oz

    VetOne Sanctuary Hand Soap - 1 Gal

  • INGREDIENTS AND APPEARANCE
    VETONE 
    vetone sanctuary foaming antibacterial hand soap liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:13985-763
    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:13985-763-160.75 L in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product11/04/202009/05/2025
    2NDC:13985-763-013.78 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/04/202012/16/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)11/04/202009/05/2025
    Labeler - MWI/VETONE (019926120)
    Registrant - Preserve International (808154199)
    Establishment
    NameAddressID/FEIBusiness Operations
    Preserve International808154199manufacture(13985-763) , api manufacture(13985-763)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!