IODINE by United Agriculture & Veterinary Products, Inc/Centaur, Inc. IODINE solution

IODINE by

Drug Labeling and Warnings

IODINE by is a Animal medication manufactured, distributed, or labeled by United Agriculture & Veterinary Products, Inc/Centaur, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

INDICATIONS & USAGE

Antiseptic/Disinfectant

For animal use only.

Keep out of reach of children.

INDICATIONS

Use as a topical antiseptic for superficial cuts, wounds, abrasions, insect bites and bruises on the skin of cattle, horses, dogs, sheep and swine.

Topical Antiseptic

For use as a counter-irritant in chronic inflammatory conditions.

DIRECTIONS

If necessary, clip hair from area to be treated and cleanse with soap and water. Apply IODINE TINCTURE 2% not more than once daily. If repeated, dilute with 3 volumes of water. Do not bandage.

DOSAGE FORMS & STRENGTHS

ACTIVE INGREDIENTS

Iodine .................................. 2%
Sodium Iodide ...................... 2%
Isopropyl Alcohol ................. 47%

INERT INGREDIENTS

Water ................................. 49%

WARNINGS AND PRECAUTIONS

POISON

First Aid: In case of ingestion, call Poison Control 1-800-222-1222

CAUTION

If redness, irritation or swelling persists or increases, discontinue use. Avoid contact with eyes and mucous membranes. Not for burns, deep wounds or body cavities.

WARNING! FLAMMABLE!

KEEP AWAY FROM HEAT AND OPEN FLAME.

KEEP CONTAINER CLOSED WHEN NOT IN USE.

STORAGE AND HANDLING

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PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

IODINE  
iodine solution

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 58305-030
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4)	IODINE	0.02 mg  in 1 mL
SODIUM IODIDE (UNII: F5WR8N145C) (IODIDE ION - UNII:09G4I6V86Q)	IODIDE ION	0.02 mg  in 1 mL
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	0.47 mg  in 1 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58305-030-80	3785 mL in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		12/12/2011

Labeler - United Agriculture & Veterinary Products, Inc/Centaur, Inc. (174239087)