NITROFURAZONE SOLUBLE DRESSING
|Category||DEA Schedule||Marketing Status|
|OTC ANIMAL DRUG LABEL||Abbreviated New Animal Drug Application|
For the prevention or treatment of surface bacterial infections of wounds, burns, and cutaneous ulcers.
Apply directly on the lesion with a spatula, or first place on a piece of gauze. Application of a bandage is optional.
This preparation should be in contact with the lesion for at least 24 hours. The dressing may be changed several times daily or left on the lesion for a longer period.
In case of deep or puncture wounds or serious burns, use only as recommended by a veterinarian. If redness, irritation, or swelling persists or increases, discontinue use, reconsult veterinarian. Avoid exposure to alkaline material and fluorescent lighting.KEEP AWAY FROM EXCESSIVE HEAT OR DIRECT SUNLIGHT.
0.2% Nitrofurazone in a Water-soluble base of Polyethylene Glycols.
Do not use in horses intended for human consumption.
CARCINOGENESIS: NITROFURAZONE, THE ACTIVE INGREDIENT OF NITROFURAZONE SOLUBLE DRESSING, HAS BEEN SHOWN TO PRODUCE MAMMARY TUMORS IN RATS AND OVARIAN TUMORS IN MICE.
SOME PEOPLE MAY BE HYPERSENSITIVE TO THIS PRODUCT. EITHER WEAR GLOVES WHEN APPLYING, OR WASH HANDS AFTERWARDS.
Store at controlled room temperature between 15°-30°C (59°-86°F). Keep container tightly closed when not In use.
For Use In Horses Only
An Antibacterial Preparation for Topical Application
CAUTION: FEDERAL LAW PROHIBITS THE USE OF THIS PRODUCT IN FOOD-PRODUCING ANIMALS.
FOR ANIMAL USE ONLY
KEEP OUT OF REACH OF CHILDREN
Distributed By: VEDCO, INC., St. Joseph, MO 64507
|Labeler - VEDCO INCORPORATED (021634266)|