Relief by Bayer HealthCare LLC RELIEF spray

Relief by

Drug Labeling and Warnings

Relief by is a Animal medication manufactured, distributed, or labeled by Bayer HealthCare LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

FRONT PANEL

NDC: 0859-2381-01

Relief®

Spray

1% Pramoxine HCl

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

WARNING: Keep out of reach of children
Anti-itch

Net Contents: 237mL (8 fl oz)

KEY INGREDIENTS:

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

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:

For temporary relief of Itching, flaking and irritation.

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.

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:

Store at room temperature. Protect from freezing.

Bayer, the Bayer Cross, DVM & Design and Relief are registered trademarks of Bayer.

Manufactured for Bayer Healthcare, LLC, Animal Health Division, Shawnee Mission, KS 66201

Made in Canada
®2017
LV1711

PACKAGE/LABEL PRINCIPAL DISPLAY PANEL

NDC: 0859-2381-01

Relief®

Spray

1% Pramoxine HCl

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

WARNING: Keep out of reach of children.

Anti-itch

Net Contents: 237 mL (8 fl oz)

INGREDIENTS AND APPEARANCE

RELIEF 
relief spray

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 0859-2381
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: 0859-2381-01	237 mL in 1 BOTTLE, PLASTIC

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

Labeler - Bayer HealthCare LLC (152266193)