EQUISHIELD IBH- chlorhexidine gluconate, ketoconazole, pramoxine hydrochloride, citronella, hydrocortisone spray

EquiShield IBH by

Drug Labeling and Warnings

EquiShield IBH by is a Animal medication manufactured, distributed, or labeled by Kinetic Technologies. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients:

Chlorhexidine Gluconate 2% (w/w)

Pramoxine HCL 1% (w/w)

Citronella Oil 1% (w/w)

Hydrocortisone 0.5% (w/w)

Purpose

Antiseptic

Topical Anesthetic

Insect Repellent

Anti-inflammatory

Uses:

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 in horses, dogs and cats.

Warnings:

For external use only.
Avoid contact with eyes and mucous membranes.
Consult your veterinarian before use.

Keep out of reach of children.

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.

EquiSheild IBH Spray, 473ml (

51031-018-06)

INGREDIENTS AND APPEARANCE

EQUISHIELD IBH 
chlorhexidine gluconate, ketoconazole, pramoxine hydrochloride, citronella, hydrocortisone spray

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 51031-018
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E) (CHLORHEXIDINE - UNII:R4KO0DY52L)	CHLORHEXIDINE GLUCONATE	2 mg  in 100 mL
PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056)	PRAMOXINE HYDROCHLORIDE	1 mg  in 100 mL
CITRONELLA OIL (UNII: QYO8Q067D0) (CITRONELLA OIL - UNII:QYO8Q067D0)	CITRONELLA OIL	1 mg  in 100 mL
HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ)	HYDROCORTISONE	0.5 mg  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51031-018-06	473 mL in 1 BOTTLE, SPRAY

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		04/06/2015

Labeler - Kinetic Technologies (164935731)