UDDERBLEND EFC 10 - 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.

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UdderBlend EFC 10

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



Blank Label



UDDERBLEND EFC 10 
iodine liquid
Product Information
Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:48106-1310
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4) IODINE55 g  in 1 L
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:48106-1310-5208 L in 1 DRUM
2NDC:48106-1310-356.8 L in 1 DRUM
3NDC:48106-1310-61040 L in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other12/01/2013
Labeler - BouMatic, LLC (124727400)
Registrant - BouMatic, LLC (124727400)
Establishment
NameAddressID/FEIBusiness Operations
BouMatic, LLC124727400api manufacture, manufacture

Revised: 12/2013
Document Id: cf142a51-8f38-4e0a-8648-1cebb6879d97
Set id: 444f49bd-dff0-4359-aa19-a9e7a0b56102
Version: 3
Effective Time: 20131201
 
BouMatic, LLC