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

  • NDC Code(s): 51031-017-01, 51031-017-04
  • 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 2, 2020

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  • Active Ingredients:

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

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

    Citronella Oil....................... 1% (w/w)............Insect Repellent

    Hydrocortisone .................0.5% (w/w).........Anti-Inflammatory

  • Indications:

    EquiShield® IBH Salve is formulated to address insect bite hypersensitivity (IBH) allergic dermatitis. EquiShield® IBH is formulated to be a topical anesthetic with antiseptic and anti-inflammatory properties and a natural insect repellant.  For use on horses.

  • Directions:

    Apply directly to the affected areas as directed by your veterinarian.

  • Warnings:

    For external use only.

    Keep out of reach of children.

    Avoid contact with eyes or mucous membranes.

    Consult your veterinarian before use.

  • Other Information:

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

  • SPL UNCLASSIFIED SECTION

    Made in U.S.A.

    KINETIC™

    P.O. Box 12388, Lexington, KY 40583

    877.786.9882 • Fax: 859.258.9177

    www.KineticVet.com

  • KINETIC™VET

    EquiShield®

    IBH

    SALVE

    Insect Bite Hypersensitivity

    FOR VETERINARY USE ONLY • KEEP OUT OF THE REACH OF CHILDREN

    Net Contents: 4 oz (113 g)

    image description

  • INGREDIENTS AND APPEARANCE
    EQUISHIELD IBH SALVE 
    chlorhexidine gluconate, pramoxine hydrochloride, citronella, hydrocortisone salve
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:51031-017
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E) (CHLORHEXIDINE - UNII:R4KO0DY52L) CHLORHEXIDINE GLUCONATE2 g  in 100 g
    PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056) PRAMOXINE HYDROCHLORIDE1 g  in 100 g
    CITRONELLA OIL (UNII: QYO8Q067D0) (CITRONELLA OIL - UNII:QYO8Q067D0) CITRONELLA OIL1 g  in 100 g
    HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE0.5 g  in 100 g
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:51031-017-04113 g in 1 CONTAINER
    2NDC:51031-017-01453 g in 1 CONTAINER
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other04/06/2015
    Labeler - Kinetic Technologies, LLC (164935731)