EQUISHIELD CK HC- chlorhexidine, ketoconazole, hydrocortisone spray

EquiShield CK HC by

Drug Labeling and Warnings

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

Drug Details [pdf]

Drug Facts:

Active Ingredients:

Chlorhexidine Gluconate ........... 2% (w/v)......................Antiseptic
Ketoconazole ........................... 1% (w/v).....................Antifungal
Hydrocortisone ...................... 0.5% (w/v)........Anti-inflammatory

Indications:

For dermatological conditions responsive to Chlorhexidine and Ketoconazole.  May be used for skin conditions with an inflammatory component.  For use on horses, dogs and cats.

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: 51031-027-08

NDC: 51031-027-06

Made in U.S.A.

#9007-03-01

#9007-03-00

KINETIC™

P.O. Box 12388, Lexington, KY 40583

877.786.9882 Fax: 859.258.9177

www.KineticVet.com

KINETICVET®

EquiShield® CK HC SPRAY

Chlorhexidine Gluconate 2%

Ketoconazole 1%

Hydrocortisone 0.5%

Antisptic & Anti-inflammatory Spray

FOR VETERINARY USE ONLY

KEEP OUT OF THE REACH OF CHILDREN

Net Contents: 8 fl oz (236 ml)

Net Contents: 16 fl oz (473 ml)

INGREDIENTS AND APPEARANCE

EQUISHIELD CK HC 
chlorhexidine, ketoconazole, hydrocortisone spray

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 51031-027
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E) (CHLORHEXIDINE - UNII:R4KO0DY52L)	CHLORHEXIDINE GLUCONATE	20 mg  in 1 mL
KETOCONAZOLE (UNII: R9400W927I) (KETOCONAZOLE - UNII:R9400W927I)	KETOCONAZOLE	10 mg  in 1 mL
HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ)	HYDROCORTISONE	5 mg  in 1 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51031-027-08	236 mL in 1 BOTTLE, SPRAY
2	NDC: 51031-027-06	473 mL in 1 BOTTLE, SPRAY

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		08/01/2023

Labeler - Kinetic Technologies, LLC (164935731)

Registrant - Kinetic Technologies LLC (164935731)