KENDALL ANTIMICROBIAL CLEANSER (BENZALKONIUM CHLORIDE) LIQUID [COVIDIEN INC.]

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KENDALL ANTIMICROBIAL CLEANSER (BENZALKONIUM CHLORIDE) LIQUID [COVIDIEN INC.]
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NDC 28851-691-01, 28851-691-02
Set ID b0fc92ba-38f6-4bef-9989-f14614003ae3
Category HUMAN OTC DRUG LABEL
Packager Covidien Inc.
Generic Name
Product Class
Product Number
Application Number PART333A
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  • 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.


  • KEEP OUT OF REACH OF CHILDREN


  • 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 TypeHUMAN OTC DRUGItem Code (Source)NDC:28851-691
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Benzalkonium Chloride (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) Benzalkonium Chloride0.13 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    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 CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:28851-691-01118 mL in 1 BOTTLE, SPRAY
    2NDC:28851-691-02236 mL in 1 BOTTLE, SPRAY
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A04/05/2011
    Labeler - Covidien Inc. (805770828)
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