EQUISHIELD IR- pramoxine, hydrocortisone spray

EquiShield IR by

Drug Labeling and Warnings

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

Drug Details [pdf]

Drug Facts:

Active Ingredients:

Pramoxine Hydrochloride .. 1% (w/w)
Hydrocortisone .................. 1% (w/w)

Purpose

..... Topical Anesthetic
..... Anti-inflammatory

Uses:

EquiShield™ IR (Itch Relief) Spray is a soothing anti-inflammatory formulation that contains Pramoxine and micronized colloidal oatmeal, combined with Hydrocortisone for the temporary relief of itching, flaking and inflammation. The EquiShield™ IR Spray formulation starts with a moistening base for a long-lasting soothing effect. Added coat conditioners and Omega-6 Essential Fatty Acids nourish the skin and help control irritation. For use on horses, dogs and cats.

Cautions:

For topical use on animals only. If redness or irritation persists or increases, discontinue use and consult your veterinarian. Avoid contact with eyes or open wounds. If contact with eyes occurs, flush thoroughly with water and consult a veterinarian.

KEEP OUT OF THE REACH OF CHILDREN

Directions:

SHAKE WELL BEFORE USE. Spray directly onto the affected skin area(s). If necessary, part the hair to ensure direct contact with the skin. Rub in well. May be used daily or as directed by veterinarian.

Other Information:

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

Package Labeling:

INGREDIENTS AND APPEARANCE

EQUISHIELD IR 
pramoxine, hydrocortisone spray

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 51031-015
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PRAMOXINE (UNII: 068X84E056) (PRAMOXINE - UNII:068X84E056)	PRAMOXINE	10 mg  in 1 mL
HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ)	HYDROCORTISONE	10 mg  in 1 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51031-015-08	236 mL in 1 BOTTLE, SPRAY

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		04/21/2015

Labeler - Kinetic Technologies (164935731)