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Kendall Antimicrobial Cleanser (Covidien Inc.)

Available Formats

Dosage Form Package Information Links
LIQUID 118 mL in 1 BOTTLE, SPRAY (28851-691-01) Label Information
LIQUID 236 mL in 1 BOTTLE, SPRAY (28851-691-02) Label Information

Complete Kendall Antimicrobial Cleanser Information

  • ACTIVE INGREDIENT

    Active Ingredient

    Benzalkonium Chloride 0.13%


  • PURPOSE

    Purpose

    Antiseptic


  • INDICATIONS & USAGE

    Use

    • a no-rinse topical antiseptic that protects against microbial contamination
    • ideal for chapped or lightly traumatized skin

  • WARNINGS

    Warnings

    For external use only.

    When using this product 
    • do not get into eyes
    Do not use on 
    • deep or puncture wounds
    • animal bites
    • serious burns
    Stop use and ask a doctor if condition worsens or symptoms last more than seven days.

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



  • DOSAGE & ADMINISTRATION

    Directions

    • spray soiled or odorous areas
    • gently wipe clean. Repeat as necessary.
    • pat dry.  No rinse necessary.
    • apply Kendall Moisturizing Lotion, Moisture Barrier Cream or Soothing Ointment as necessary

  • SPL UNCLASSIFIED SECTION

    Other Information

    • protect from freezing
    • avoid excessive heat

  • INACTIVE INGREDIENT

    Inactive ingredients

    Water, Polysorbate 20, linoleamidopropyl PG-dimonium chloride phosphate, propylene glycol, cirtus aurantium bergamia (bergamot) fruit oil, citrus medica vulgaris peel oil, retinyl palmitate, tocopheryl acetate, methylparaben, propylparaben, diazolidinyl urea


  • QUESTIONS

    Questions or comments?  1-800-962-9888


  • PRINCIPAL DISPLAY PANEL

    Image of 4 Ounce Label

    Image of Kendall Antimicrobial Cleanser Label


  • INGREDIENTS AND APPEARANCE
    KENDALL ANTIMICROBIAL CLEANSER 
    benzalkonium chloride liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:28851-691
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Benzalkonium Chloride (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) Benzalkonium Chloride 0.13 mL  in 100 mL
    Inactive Ingredients
    Ingredient Name Strength
    Water (UNII: 059QF0KO0R)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    PHOSPHATE ION (UNII: NK08V8K8HR)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    BERGAMOT OIL (UNII: 39W1PKE3JI)  
    VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
    ACETATE ION (UNII: 569DQM74SC)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:28851-691-01 118 mL in 1 BOTTLE, SPRAY
    2 NDC:28851-691-02 236 mL in 1 BOTTLE, SPRAY
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333A 04/05/2011
    Labeler - Covidien Inc. (805770828)