Label: EQUISHIELD CK HC- chlorhexidine, ketoconazole, hydrocortisone spray

  • NDC Code(s): 51031-027-06, 51031-027-08
  • Packager: Kinetic Technologies, LLC
  • Category: OTC ANIMAL DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated August 28, 2023

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  • Drug Facts:

  • Active Ingredients:

    Chlorhexidine Gluconate ........... 2% (w/v)......................Antiseptic
    Ketoconazole ........................... 1% (w/v).....................Antifungal
    Hydrocortisone ...................... 0.5% (w/v)........Anti-inflammatory

  • Indications:

    For dermatological conditions responsive to Chlorhexidine and Ketoconazole.  May be used for skin conditions with an inflammatory component.  For use on horses, dogs and cats.

  • Warnings:

    For external use only.
    Avoid contact with eyes and mucous membranes.
    Keep out of reach of children.
    Consult your veterinarian before use.

  • Directions:

    Apply directly to affected areas as directed by your veterinarian.

  • Other Information:

    • Store at room temperature 15˚ - 30˚C (58˚ - 86˚F).
    • Store in a cool, dry place.

  • SPL UNCLASSIFIED SECTION

    NDC 51031-027-08

    NDC 51031-027-06

    Made in U.S.A.

    #9007-03-01

    #9007-03-00

    KINETIC™

    P.O. Box 12388, Lexington, KY 40583

    877.786.9882 • Fax: 859.258.9177

    www.KineticVet.com

  • KINETICVET®

    EquiShield® CK HC SPRAY

    Chlorhexidine Gluconate 2%

    Ketoconazole 1%

    Hydrocortisone 0.5%

    Antisptic & Anti-inflammatory Spray

    FOR VETERINARY USE ONLY

    KEEP OUT OF THE REACH OF CHILDREN

    Net Contents: 8 fl oz (236 ml)

    Net Contents: 16 fl oz (473 ml)

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  • INGREDIENTS AND APPEARANCE
    EQUISHIELD CK HC 
    chlorhexidine, ketoconazole, hydrocortisone spray
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:51031-027
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E) (CHLORHEXIDINE - UNII:R4KO0DY52L) CHLORHEXIDINE GLUCONATE20 mg  in 1 mL
    KETOCONAZOLE (UNII: R9400W927I) (KETOCONAZOLE - UNII:R9400W927I) KETOCONAZOLE10 mg  in 1 mL
    HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE5 mg  in 1 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:51031-027-08236 mL in 1 BOTTLE, SPRAY
    2NDC:51031-027-06473 mL in 1 BOTTLE, SPRAY
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other08/01/2023
    Labeler - Kinetic Technologies, LLC (164935731)
    Registrant - Kinetic Technologies LLC (164935731)
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