SCARLET OIL WOUND DRESSING- scarlet oil solution

Scarlet Oil by

Drug Labeling and Warnings

Scarlet Oil by is a Animal medication manufactured, distributed, or labeled by Durvet, Inc., FIRST PRIORITY INCORPORATED. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PURPOSE

For Simple Wounds, Cuts and Abrasions

ACTIVE INGREDIENT

Active Ingredient 0.3% (w/w) PCMX (Parachlorometaxylenol)

KEEP OUT OF REACH OF CHILDREN

FOR ANIMAL USE ONLY

KEEP OUT OF REACH OF CHILDREN

INDICATIONS:

For use as a dressing for simple wounds, cuts and abrasions on horses and mules.

WARNING:

Not for use on animals intended for food.

CAUTION:

Use only as directed. Avoid contact with eyes and mucous membranes. Do not apply to large areas of broken skin. In case of deep or puncture wounds or serious burns, consult a veterinarian. If redness, irritation, or swelling persists or increases, discontinue use and consult a veterinarian.

DIRECTIONS FOR USE:

Clean the affected area, clipping hair if necessary. Direct spray at the site to be treated. Hold container 4 to 6 inches from animal. Apply freely as an open wound treatment or wrap with a clean bandage. Treatment may be applied once or twice daily.

INACTIVE INGREDIENTS:

Mineral Oil, Isopropyl Alcohol, Methyl Salicylate, Benzyl Alcohol, Pine Oil, Eucalyptus Oil and Biebrich Scarlet Red.

STORAGE:

Store at controlled room temperature between 15º-30ºC (59º-86ºF). Keep container tightly closed when not in use.

WARNINGS AND PRECAUTIONS

The following statement is made in compliance with the State of California Agricultural Code: Not For Human Use.

WARNING! FLAMMABLE! KEEP AWAY FROM HEAT AND OPEN FLAME.

Net Contents:

16 fl oz (473 mL)

INFORMATION FOR OWNERS/CAREGIVERS

Manufactured for:
DURVET, INC.
Blue Springs, Missouri 64014

www.durvet.com

Net Contents: 16 fl oz (473 mL)

INGREDIENTS AND APPEARANCE

SCARLET OIL  WOUND DRESSING
scarlet oil solution

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 30798-626
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	2.5 mg  in 1 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 30798-626-31	12 in 1 CASE
1		473 mL in 1 BOTTLE

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

Labeler - Durvet, Inc. (056387798)

Establishment
Name	Address	ID/FEI	Business Operations
FIRST PRIORITY INCORPORATED		179925722	manufacture, label