RELIEF- pramoxine hydrochloride spray

Relief by

Drug Labeling and Warnings

Relief by is a Animal medication manufactured, distributed, or labeled by Elanco US Inc., Syn-Tech Chem. & Pharm. Co., Ltd., Groupe PARIMA Inc., Tropichem Research Labs, LLC dba Vetio. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

KEY INGREDIENTS: Pramoxine Hydrochloride 1%, Omega-6 fatty acids and colloidal oatmeal.

DESCRIPTION

PRODUCT DESCRIPTION: Relief Spray combines the soothing benefits of pramoxine and colloidal oatmeal in a moisturizing base that remains on the skin for anti-itch activity. It contains Omega-6 fatty acids for nourishment of the skin.

INDICATIONS & USAGE

INDICATIONS: For temporary relief of itching, flaking and irritation.

DOSAGE & ADMINISTRATION

DIRECTIONS: Shake well before use. Spray directly onto the affected areas. If necessary, part hair coat so that Relief Spray makes direct contact with the skin. Rub in well. May be used daily or as directed by your veterinarian.

SPL UNCLASSIFIED SECTION

CAUTIONS: For topical use on dogs, cats, and horses only. If redness or irritation persists or increases, discontinue use and contact your veterinarian. Avoid contact with eyes. If eye contact occurs, rinse thoroughly with water.

STORAGE AND HANDLING

STORAGE: Store at room temperature. Protect from freezing.

Manufactured for Elanco US Inc.
Greenfield, IN 46140 U.S.A.
DVM & Design and Relief, Elanco and the diagonal bar logo
are trademarks of Elanco or its affiliates.
© 2022 Elanco or its affiliates

DVM™

Elanco™

90210026_YL600283B

Principal Display Panel – 237 mL Bottle Spray Label

Elanco™

Relief™
SPRAY

Colloidal oatmeal spray
for temporary relief of itching and
flaking on dogs, cats, and horses.

1% Pramoxine HCl

WARNING: Keep out of reach of children.

Anti-itch

NET CONTENTS 237mL (8 fl oz)

INGREDIENTS AND APPEARANCE

RELIEF 
pramoxine hydrochloride spray

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 58198-0014
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056)	PRAMOXINE HYDROCHLORIDE	10.8 mg  in 1 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58198-0014-1	1 in 1 BOTTLE, SPRAY
1		237 mL in 1 BOTTLE, SPRAY

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Unapproved drug other		02/15/2017

Labeler - Elanco US Inc. (966985624)