UDDERBLEND EFC 10- iodine liquid

UdderBlend EFC 10 by

Drug Labeling and Warnings

UdderBlend EFC 10 by is a Animal medication manufactured, distributed, or labeled by BouMatic, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

INDICATIONS & USAGE

Concentrate for 1.0% Iodine Teat Dip

Helps reduce the spread of organisms which may cause Mastitis

NOT FOR HUMAN USE

FOR EXTERNAL USE ONLY

USE DIRECTIONS: Do not use in concentrated form. Must dilute prior to use.

Consult your BouMatic representative for specific use
instructions and recommended dispensing equipment.


Active Ingredient (Iodine 5.0%.)

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

UDDERBLEND EFC 10 
iodine liquid

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 48106-1310
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4)	IODINE	55 g  in 1 L

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 48106-1310-5	208 L in 1 DRUM
2	NDC: 48106-1310-3	56.8 L in 1 DRUM
3	NDC: 48106-1310-6	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		12/01/2013

Labeler - BouMatic, LLC (124727400)

Registrant - BouMatic, LLC (124727400)

Establishment
Name	Address	ID/FEI	Business Operations
BouMatic, LLC		124727400	api manufacture, manufacture