Label: UDDERBLEND EFC 10- iodine liquid
- NDC Code(s): 48106-1310-3, 48106-1310-5, 48106-1310-6
- Packager: BouMatic, LLC
- Category: OTC ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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.
Drug Label Information
Updated December 1, 2013
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
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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
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INGREDIENTS AND APPEARANCE
UDDERBLEND EFC 10
iodine liquidProduct 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
