UDDERBLEND EFC 5 - 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 5

Concentrate for 0.5% 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 5 
iodine liquid
Product Information
Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:48106-1305
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:48106-1305-5208 L in 1 DRUM
2NDC:48106-1305-356.8 L in 1 DRUM
3NDC:48106-1305-61040 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: 83533719-d0ac-4ca2-9351-9b7f2593a9b1
Set id: f7b13f0a-4341-49b3-a8e4-fe72e0811329
Version: 3
Effective Time: 20131201
 
BouMatic, LLC