Label: CONTROLLED IODINE- iodine solution
- NDC Code(s): 30798-466-31, 30798-466-35
- Packager: Durvet Inc
- Category: OTC ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated August 14, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
-
INDICATIONS & USAGE
Controlled Iodine Spray
Antiseptic/Disinfectant
For Skin Disinfection, Superficial Wounds, Navel Cords
FOR ANIMAL USE ONLY
KEEP OUT OF REACH OF CHILDREN
INDICATIONS: In cattle, horses, swine and sheep as a topical antiseptic for use prior to surgical procedures such as castraing and docking; for ringworms and foot rot; for application to the naveal of newborn animals; and for minor cuts, teat sores, bruises and abraissions.
-
DIRECTIONS:
Remove spray cap from 16 oz. container and refill from gallon container. Replace spray cap tightly. Hold container approximately 4 to 8 inches from the area to be sprayed. Point valve at the area to be sprayed. Pull trigger of valve and spray area once lightly. May be repeated daily, if necessary, until the 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 the milk.
- INGREDIENTS:
- STORAGE
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
CONTROLLED IODINE
iodine solutionProduct 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