Label: UDDERSTAR BARRIER ACTIVATOR- sodium chlorite teat dip liquid

  • NDC Code(s): 43104-2017-1, 43104-2017-2, 43104-2017-3, 43104-2017-4, view more
    43104-2017-5, 43104-2017-6
  • Packager: Knapp Manufacturing, Inc.
  • Category: OTC ANIMAL DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated February 20, 2023

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  • Summary of effectiveness

    Helps reduce the spread of organisms which may
    cause Mastitis

  • Instructions for use

    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.

  • Safe Handling

    NOT FOR HUMAN USE
    FOR EXTERNAL USE ONLY
    Do not mix with any chemicals other than UdderStar Barrier Base.
    In a well-ventilated area, mix equal parts UdderStar Barrier Activator and UdderStar Barrier

  • General Precautions

    CAUTION
    KEEP OUT OF REACH OF CHILDREN
    NOT FOR HUMAN USE

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

  • Storage and Handling

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

  • label

    label

  • INGREDIENTS AND APPEARANCE
    UDDERSTAR BARRIER ACTIVATOR 
    sodium chlorite teat dip liquid
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:43104-2017
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LACTIC ACID (UNII: 33X04XA5AT) (LACTIC ACID - UNII:33X04XA5AT) LACTIC ACID10 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    SORBITOL (UNII: 506T60A25R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:43104-2017-13914 g in 1 PACKAGE
    2NDC:43104-2017-219570 g in 1 PACKAGE
    3NDC:43104-2017-358710 g in 1 PACKAGE
    4NDC:43104-2017-4117421 g in 1 PACKAGE
    5NDC:43104-2017-5215271 g in 1 PACKAGE
    6NDC:43104-2017-61076359 g in 1 PACKAGE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other02/20/2023
    Labeler - Knapp Manufacturing, Inc. (063012827)
    Establishment
    NameAddressID/FEIBusiness Operations
    Knapp Manufacturing, Inc.063012827api manufacture
    Establishment
    NameAddressID/FEIBusiness Operations
    BouMatic, LLC124727400manufacture
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Safety

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Clinical Trials, PubMed, Biochemical Data Summary

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