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

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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)

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  • 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)