UDDERBLEND EFC 10 NPE FREE- iodine teat dip liquid

Udderblend EFC 10 NPE Free by

Drug Labeling and Warnings

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

Drug Details [pdf]

WARNINGS AND 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

INDICATIONS & USAGE

CONCENTRATE FOR 1% 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%.)

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

UDDERBLEND EFC 10 NPE FREE 
iodine teat dip liquid

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 48106-2001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Iodine (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4)	Iodine	53 g  in 1 L

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 48106-2001-1	56.8 L in 1 DRUM
2	NDC: 48106-2001-2	208 L in 1 DRUM
3	NDC: 48106-2001-3	1041 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		08/01/2015

Labeler - BouMatic, LLC (124727400)

Establishment
Name	Address	ID/FEI	Business Operations
Boumatic		080073197	manufacture, api manufacture