Label: EQUISHIELD IBH- chlorhexidine gluconate, pramoxine hydrochloride, citronella, hydrocortisone spray

  • NDC Code(s): 51031-018-06
  • 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 December 10, 2020

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  • Active Ingredients:

    Chlorhexidine Gluconate ........... 2% (w/v)...................... Antiseptic

    Pramoxine HCL ........................ 1% (w/v)........... Topical Anesthetic

    Citronella Oil ........................... 1% (w/v).............. Insect Repellant

    Hydrocortisone ..................... 0.5% (w/v)........... Anti-inflammatory

  • Properties:

    EquiShield® IBH Spray is formulated to address Insect Bite Hypersensitivity allergic dermatitis. Formulated to be a topical anesthetic with antiseptic and anti-inflammatory properties, EquiShield® IBH Spray soothes and treats the horse while naturally repelling insects. For use on horses.

  • 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 51031-018-06

    Made in U.S.A.

    #9009-03-00

    KINETIC™

    P.O. Box 12388, Lexington, KY 40583

    877.786.9882 • Fax: 859.258.9177

    www.KineticVet.com

  • KINETIC™VET

    EquiShield®​

    IBH

    SPRAY

    Insect Bite Hypersensitivity

    FOR VETERINARY USE ONLY

    KEEP OUT OF THE REACH OF CHILDREN

    Net Contents: 16 fl oz (473 ml)

    image description

  • INGREDIENTS AND APPEARANCE
    EQUISHIELD IBH 
    chlorhexidine gluconate, pramoxine hydrochloride, citronella, hydrocortisone spray
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:51031-018
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E) (CHLORHEXIDINE - UNII:R4KO0DY52L) CHLORHEXIDINE GLUCONATE2 g  in 100 mL
    PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056) PRAMOXINE HYDROCHLORIDE1 g  in 100 mL
    CITRONELLA OIL (UNII: QYO8Q067D0) (CITRONELLA OIL - UNII:QYO8Q067D0) CITRONELLA OIL1 g  in 100 mL
    HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE0.5 g  in 100 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:51031-018-06473 mL in 1 BOTTLE, SPRAY
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other04/06/2015
    Labeler - Kinetic Technologies, LLC (164935731)
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