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Kendall Soothing (Covidien Inc.)

Available Formats

Dosage Form Package Information Links
OINTMENT 118 mL in 1 TUBE (28851-695-02) Label Information
OINTMENT 59 mL in 1 TUBE (28851-695-01) Label Information
OINTMENT 4 mL in 1 POUCH (28851-695-03) Label Information

Complete Kendall Soothing Information

  • ACTIVE INGREDIENT

    Active Ingredient

    Zinc oxide 10%


  • PURPOSE

    Purpose

    Skin protectant


  • INDICATIONS & USAGE

    Use

    temporarily protects chapped or cracked 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
    • symptoms last more than seven days or clear up and occur again within a few days.
    Keep out of the reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.



  • DOSAGE & ADMINISTRATION

    Directions

    • apply as needed

  • SPL UNCLASSIFIED SECTION

    Other Information

    • protect from freezing
    • avoid excessive heat

  • INACTIVE INGREDIENT

    Inactive ingredients

    Water, Polysorbate 60, petrolatum, sorbitan stearate, cetyl alcohol, propylene glycol, dimethicone, simmondsia chinensis (jojoba) seed oil, decylene glycol, xanthan gum, cetyl hydroxyethylcellulose, citrus 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 Kendall Soothing Ointment 2 Fl oz Label

    Image of Kendall Soothing Ointment 2 Fl oz Label






  • INGREDIENTS AND APPEARANCE
    KENDALL SOOTHING 
    zinc oxide ointment
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:28851-695
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Zinc Oxide (UNII: SOI2LOH54Z) (Zinc - UNII:J41CSQ7QDS) Zinc Oxide 10 mL  in 100 mL
    Inactive Ingredients
    Ingredient Name Strength
    Water (UNII: 059QF0KO0R)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)  
    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)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    JOJOBA OIL (UNII: 724GKU717M)  
    POLYSORBATE 60 (UNII: CAL22UVI4M)  
    1-DECENE (UNII: 7O4U4C718P)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    CETYL HYDROXYETHYLCELLULOSE (350000 MW) (UNII: T7SWE4S2TT)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:28851-695-01 59 mL in 1 TUBE
    2 NDC:28851-695-02 118 mL in 1 TUBE
    3 NDC:28851-695-03 4 mL in 1 POUCH
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part347 04/22/2011
    Labeler - Covidien Inc. (805770828)