UDDERDINE 105- iodine liquid

Udderdine 105 by

Drug Labeling and Warnings

Udderdine 105 by is a Animal medication manufactured, distributed, or labeled by BouMatic, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

INDICATIONS & USAGE

Helps reduce the spread of organisms which may cause Mastitis

USE DIRECTIONS

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

PRE-DIPPING: Before milking, dip or spray entire teat with this product. Wipe teats dry after application using single-service towels to avoid contamination of milk.

POST-DIPPING: After milking, spray or 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.

PRECAUTIONS

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

UDDERDINE 105 
iodine liquid

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 48106-1100
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4)	IODINE	10 g  in 1 L

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 48106-1100-1	3.8 L in 1 DRUM
2	NDC: 48106-1100-2	18.9 L in 1 DRUM
3	NDC: 48106-1100-3	56.8 L in 1 DRUM
4	NDC: 48106-1100-4	114 L in 1 DRUM
5	NDC: 48106-1100-5	208 L in 1 DRUM
6	NDC: 48106-1100-6	1040 L in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK

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	Business Operations
BouMatic, LLC		124727400	manufacture, api manufacture