Bovi-Kote: Product Information

BOVI-KOTE — iodine liquid
BouMatic, LLC

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.

Helps reduce the spread of organisms which may cause Mastitis

USE DIRECTIONS

NOT FOR HUMAN USE
FOR EXTERNAL USE ONLY
USE AT FULL STRENGTH

POST-DIPPING: After milking, dip entire teat with this product. Allow to air dry.
Note: If solution in cup becomes visibly dirty, replenish with a fresh mixture of this product. Do not return unused product to original container.

CAUTION

KEEP OUT OF REACH OF CHILDREN
NOT FOR HUMAN USE
FIRST AID:
If in eyes: Hold eye open and rinse slowly and gently with water for 15-20 minutes. Remove contact lenses, if present after the first 5 minutes, then continue rinsing. Contact a physician immediately. If swallowed: Have person sip a glass of water if able to swallow. Do not give anything to an unconscious person. Do not induce vomiting. Contact a physician immediately. If breathing difficulty occurs: Move person to fresh air. Contact a physician immediately. If on skin: Take off contaminated clothing. Rinse skin with soap and water. If irritation develops and persists, contact a physician.
Have the product container or label with you when going for treatment, calling a physician, the emergency number listed on this label or MSDS, or a poison control center.
PRECAUTION: Avoid eye contact. Do not ingest. Do not mix with any chemicals except as directed.
STORAGE: Store in a closed container away from sources of heat. If product becomes frozen, thaw and mix well before use.
SEE MATERIAL SAFETY DATA SHEET

Blank Label
(click image for full-size original)

BOVI-KOTE
iodine liquid
Product Information
Product Type OTC ANIMAL DRUG Item Code (Source) NDC:48106-1116
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
IODINE (IODINE) IODINE 110 mL in 10 L
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:48106-1116-1 3.8 L in 1 DRUM None
2 NDC:48106-1116-2 18.9 L in 1 DRUM None
3 NDC:48106-1116-3 56.8 L in 1 DRUM None
4 NDC:48106-1116-4 114 L in 1 DRUM None
5 NDC:48106-1116-5 208 L in 1 DRUM None
6 NDC:48106-1116-6 1040 L in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 08/01/2007
Labeler — BouMatic, LLC (124727400)
Registrant — BouMatic, LLC (124727400)
Establishment
Name Address ID/FEI Operations
BouMatic, LLC 124727400 manufacture, api manufacture

Revised: 01/2012 BouMatic, LLC

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