Label: BULK IODINE CONCENTRATE- iodine teat dip liquid

  • Category: OTC ANIMAL DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated May 2, 2023

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  • Claim of effectiveness.

    Helps reduce the spread of organisms
    which may cause Mastitis

  • Use Directions

    NOT FOR HUMAN USE
    FOR EXTERNAL USE ONLY
    Do not use in concentrated form.
    Use only as directed.
    For use only with BouMatic mixing
    systems.
    Reference procedure manual for
    specific mixing instructions.

  • 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 SDS, or a poison control
    center.

  • Precautions & Hazards

    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.

  • label

    image description

  • INGREDIENTS AND APPEARANCE
    BULK IODINE CONCENTRATE 
    iodine teat dip liquid
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:48106-2051
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4) IODINE7.3 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:48106-2051-11076359 g in 1 PACKAGE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other05/02/2023
    Labeler - BOUMATIC, LLC (124727400)
    Establishment
    NameAddressID/FEIBusiness Operations
    BOUMATIC, LLC124727400api manufacture
    Establishment
    NameAddressID/FEIBusiness Operations
    Knapp Manufacturing, Inc.063012827manufacture
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Safety

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Clinical Trials, PubMed, Biochemical Data Summary

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