NDC | 48106-2002-1, 48106-2002-2, 48106-2002-3, 48106-2002-4 |
Set ID | 1567159f-0335-493b-bea0-b0aec8cf6f86 |
Category | OTC ANIMAL DRUG LABEL |
Packager | BouMatic, LLC |
Generic Name | |
Product Class | |
Product Number | |
Application Number |
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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
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INDICATIONS & USAGE
UdderBlend NPE Free
Iodine Teat Dip Concentrate
Helps reduce the spread of organisms which may cause Mastitis
RESTRICTED DRUG (CA) - USE ONLY AS DIRECTED
USE DIRECTIONS
NOT FOR HUMAN USE
FOR EXTERNAL USE ONLY
Do not use in concentrated form. Must dilute prior to use.
To obtain a 1% iodine solution and 2% emollients, add 1 part UdderBlend to 4 parts water and mix thoroughly.
To obtain a 0.5% iodine solution and 1% emollients, add 1 part UdderBlend to 9 parts water and mix thoroughly.
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
UDDERBLEND NPE FREE
iodine teat dip concentrate liquidProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:48106-2002 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:48106-2002-1 19 L in 1 DRUM 2 NDC:48106-2002-2 56.8 L in 1 DRUM 3 NDC:48106-2002-3 208 L in 1 DRUM 4 NDC:48106-2002-4 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