CONTROLLED IODINE- iodine solution

Controlled Iodine by

Drug Labeling and Warnings

Controlled Iodine by is a Animal medication manufactured, distributed, or labeled by Durvet Inc, Centaur Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

WARNINGS AND PRECAUTIONS

Topical Antiseptic
For animal use only.
Keep out of reach of children.

INDICATIONS
In horses, cattle, swine and sheep as a topical antiseptic for use prior to surgical procedures such as castrating and docking; for ringworm and foot rot; for application to the navel of newborn animals; and for the aid in the treatment of minor cuts, bruises, teat sores, and abrasions
For use as a counter-irritant in chronic inflammatory conditions.

DIRECTIONS
Remove spray cap from 16 oz. container and refill from gallon container. Replace spray cap tightly. Hold container approxiamately 4 to 6 inches from the area to be sprayed. Point valve at the area to be sprayed. Pull trigger and spray area once lightly. May be repeated daily, when necessary, until abraded area is healed.

CAUTION
If redness, irritation, or swelling persists or increases discontinue use and consult a veterinarian. Not for use on burns or in body cavities or deep wounds.

NOTE
When used on or near the teats or udders of dairy animals, the teats and udders should be thoroughly washed before the next milking to prevent contamination of milk.

Active Ingredients
Alpha (p-nonylphenyl) Omega-Hydroxypoly (Oxyethylene) Iodine Complex (providing 1% titratable Iodine) .................................. 5%
Inert Ingredients
Water & Nonionic Surfactant ................................. 95%

CAUTION
Harmful if swallowed. Do not apply to the eyes, mucous membranes or large areas of abraded skin. Avoid inhalation of mist.

KEEP TIGHTLY CLOSED WHEN NOT IN USE.
FOR EXTERNAL ANIMAL USE ONLY.
KEEP OUT REACH OF CHILDREN.
STORE AT 10o-30oC (50o-86oF)

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CONTROLLED IODINE 
iodine solution

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 30798-466
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4)	IODINE	0.01 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)	0.99 mg  in 1 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 30798-466-31	473 mL in 1 BOTTLE
2	NDC: 30798-466-35	3785 mL in 1 JUG

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		02/01/2012

Labeler - Durvet Inc (056387798)

Establishment
Name	Address	ID/FEI	Business Operations
Centaur Inc		174239087	api manufacture, manufacture