Label: UDDERBLEND - iodine liquid
view more48106-1160-5, 48106-1160-6
- Packager: BouMatic, LLC
- Category: OTC ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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- INDICATIONS & USAGE
IODINE TEAT DIP CONCENTRATE
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.
To obtain a 1% iodine solution and 2% emollient, add 1 gallon (4 L) of UDDERBLEND to 4 gallons (8L) of water and mix thoroughly.
To obtain a 0.5% iodine solution and 1% emollient, add 1 gallon (4 L) of UDDERBLEND to 9 gallons (19 L) of water and mix thoroughly.
PRE-DIPPING: Before milking, dip or spray entire teat with this product. Wipe teats dry after application using single-service towels to avoid contamination of milk.
POST-DIPPING: After milking, spray or dip entire teat with this product. Allow to air dry.
Note: If solution in cup becomes visibly dirty, replenish with a fresh mixture of this product. Do not return unused product to original container. Close
KEEP OUT OF REACH OF CHILDRENClose
NOT FOR HUMAN USE
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
Product Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:48106-1160 Route of Administration TOPICAL DEA Schedule Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4) IODINE 450 g in 10 L Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:48106-1160-5 208 L in 1 DRUM 2 NDC:48106-1160-6 1040 L in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK 3 NDC:48106-1160-1 3.8 L in 1 DRUM 4 NDC:48106-1160-2 18.9 L in 1 DRUM 5 NDC:48106-1160-3 56.8 L in 1 DRUM 6 NDC:48106-1160-4 114 L in 1 DRUM Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 01/01/2012 Labeler - BouMatic, LLC (124727400) Registrant - BouMatic, LLC (124727400) Establishment Name Address ID/FEI Business Operations BouMatic, LLC 124727400 api manufacture, manufacture Establishment Name Address ID/FEI Business Operations Knapp Manufacturing 063012827 api manufacture, manufacture