Label: 1%/15% ELITE IODINE BARRIER POST DIP- iodine post teat dip liquid

  • NDC Code(s): 48106-2045-1, 48106-2045-2, 48106-2045-3, 48106-2045-4, view more
    48106-2045-5, 48106-2045-6
  • 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 2, 2022

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  • Summary of effectiveness

    Helps reduce the spread of organisms which
    may cause Mastitis

  • Instructinos for use

    USE DIRECTIONS: NOT FOR HUMAN USE
    FOR EXTERNAL USE ONLY
    USE AT FULL STRENGTH
    PRE-DIPPING: Before milking, dip entire teat with
    this product. Wipe teats dry after application using
    single-service towels to avoid contamination of milk.
    POST-DIPPING: After milking, 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.

  • Safe Handling

    CAUTION
    KEEP OUT OF REACH OF CHILDREN
    NOT FOR HUMAN USE

  • General Precautions

    Avoid eye contact. Do not ingest.Do not mix with any chemicals except as directed.

    NOT FOR HUMAN USE
    FOR EXTERNAL USE ONLY
    USE AT FULL STRENGTH

  • Storage

    Store in a closed container away from sources of heat. If product becomes frozen, thaw and mix well before
    use.

  • Label

    labellabel

  • INGREDIENTS AND APPEARANCE
    1%/15% ELITE IODINE BARRIER POST DIP 
    iodine post teat dip liquid
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:48106-2045
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4) IODINE1 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 6 g  in 100 g
    SORBITOL (UNII: 506T60A25R) 2.38 g  in 100 g
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3) 3 g  in 100 g
    WATER (UNII: 059QF0KO0R) 87.62 g  in 100 g
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:48106-2045-13900 g in 1 PACKAGE
    2NDC:48106-2045-220000 g in 1 PACKAGE
    3NDC:48106-2045-359000 g in 1 PACKAGE
    4NDC:48106-2045-4118000 g in 1 PACKAGE
    5NDC:48106-2045-5216000 g in 1 PACKAGE
    6NDC:48106-2045-61081000 g in 1 PACKAGE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other12/02/2022
    Labeler - BOUMATIC, LLC (124727400)
    Establishment
    NameAddressID/FEIBusiness Operations
    BOUMATIC, LLC124727400api manufacture
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Safety

Report Adverse Events (Animal Drug), FDA Safety Recalls (Animal Drug)

Related Resources

Clinical Trials, PubMed, Biochemical Data Summary

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