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

  • Category: OTC ANIMAL DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated December 17, 2025

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  • SPL UNCLASSIFIED SECTION

    NDC 53413-018-06

    Active Ingredients:

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

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

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

    Hydrocortisone ..................... 0.5% (w/v)

    Purpose

    Antiseptic

    Topical Anesthetic

    Insect Repellent

    Anti-Inflammatory

    Inactive Ingredients:

    Ethanol, Purified Water, Polysorbate 20

    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.

    Directions:

    Apply directly to affected areas as directed by your veterinarian.

    Warnings:

    For external use only.

    Avoid contact with eyes and mucous membranes.

    Consult your veterinarian before use.

    Keep out of reach of children.

    Other Information:

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

    #9009-03-00

    REV1225 S22A

    UPC 851559000511

    Manufactured for Creative Science

    1700 Albany Place SE, Orange City, IA 51041

    888.506.3039

    www.creative.science

  • PRINCIPAL DISPLAY PANEL

    IBH Spray 16 oz

    EquiShield® IBH SPRAY

    Insect Bite Hypersensitivity

    FOR VETERINARY USE ONLY

    KEEP OUT OF THE REACH OF CHILDREN

    Net Contents: 16 fl oz (473 ml)

  • INGREDIENTS AND APPEARANCE
    EQUISHIELD IBH 
    chlorhexidine gluconate, pramoxine hydrochloride, citronella, hydrocortisone spray
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:53413-018
    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:53413-018-06473 mL in 1 BOTTLE, SPRAY
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other12/01/2025
    Labeler - Creative Science (609777461)
    Registrant - Creative Science (609777461)
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