Label: XT BARRIER BLU PART B- sodium chlorite solution

  • NDC Code(s): 17307-3006-1, 17307-3006-2, 17307-3006-3, 17307-3006-4
  • Packager: AgroChem USA, 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 September 12, 2023

If you are a consumer or patient please visit this version.

  • SPL UNCLASSIFIED SECTION

    XT BARRIER BLU PART B

  • WARNINGS

    WARNING

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN

  • WARNINGS AND PRECAUTIONS

    AVOID FREEZING.

    KEEP OUT OF DIRECT SUNLIGHT.

    CAUSES SERIOUS EYE IRRITATION.

    FOR FARM AND INDUSTRIAL USE ONLY.

    PREVENTION:  Wash skin thoroughly after handling. Wear eye protection/ face protection.

    FIRST AID / RESPONSE: 

    IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. If eye irritation persists:  Get medical advice/ attention.          

  • STORAGE AND HANDLING

    STORAGE:  Store locked up.                       

    DISPOSAL: Dispose of contents/ container to an approved waste disposal plant

  • ACTIVE INGREDIENT

    ACTIVE INGREDIENT: Sodium Chlorite 0.45%

  • SPL UNCLASSIFIED SECTION

    EMERGENCY TELEPHONE NUMBER (Chemtrec) 800-424-9300 CCN205494

    NET CONTENTS: 55 Gallons

    LOT:

    EXP. DATE:

    Use XT Barrier BLU effectively to reduce the spread of mastitis causing organisms. Recommended for pre and post milking applications.

  • INSTRUCTIONS FOR USE

    DIRECTIONS:

    IMPORTANT:  MUST BE MIXED PRIOR TO USE.  Mix PART A & PART B in equal parts.  Mix by volume.  Add  equal parts of PART A and PART B in a separate container.  Inverting the container approximately 5-7 times will adequately mix the two solutions. This mixed solution will remain stable for 7 days.  After 7 days, discard solution and mix a new solution.

    General Use

    Once mixed according to directions , do not mix product with any other teat dips, or other product.

    Use a teat dip cup to apply.  Clean dip cup just prior to use.

    If cow’s teats are sore or chapped, consult a veterinarian before starting or continuing to use teat dip.

    If transferred from this container to any other, make sure that the other container is thoroughly pre-cleaned and bears the proper container labeling for this product. 

    If product in dip cup becomes visibly dirty, discard contents and replenish with undiluted product. Do not reuse or return any unused product to the original container.

    Pre Dipping Use

    Perform forestripping and inspect teats for clinical mastitis.

    Pre-wash teats thoroughly just prior milking with appropriate udder wash solution or pre-milking teat dip. Teats should then be dried with single-service towels

    Just before each cow is milked, dip, foam, or spray, each teat full-length into the teat dip or foam cup containing product.

    Allow product to stand for 30 seconds.

    Wipe teats dry after dipping, using single-service towels to avoid contamination of milk.

    Post Dipping Use

    Immediately after each milking, use product.

    Dip each teat full-length into the teat dip cup containing product.  Allow to air dry.  Do not wipe.

    If outside temperature is below freezing, allow to air dry on the teat before cow leaves the parlor.

    Extended Use

    When a cow is being dried off, the teats should be dipped in product, once a day for 3-4 days after the last milking.

    Dipping should be resumed at least twice daily one week before calving.

  • SPL UNCLASSIFIED SECTION

    Manufactured By:

    AgroChem USA, LLC 26 Freedom Way • Saratoga Springs, NY 12866 •  (518)226-4850

  • PRINCIPAL DISPLAY PANEL

    image description

  • INGREDIENTS AND APPEARANCE
    XT BARRIER BLU PART B 
    sodium chlorite solution
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:17307-3006
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM CHLORITE (UNII: G538EBV4VF) (CHLORITE ION - UNII:Z63H374SB6) SODIUM CHLORITE0.01458 kg  in 1 kg
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:17307-3006-119 kg in 1 CONTAINER
    2NDC:17307-3006-257 kg in 1 DRUM
    3NDC:17307-3006-3208 kg in 1 DRUM
    4NDC:17307-3006-41041 kg in 1 CONTAINER
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other09/12/2023
    Labeler - AgroChem USA, LLC (118336116)
    Registrant - AgroChem USA, LLC (118336116)
    Establishment
    NameAddressID/FEIBusiness Operations
    AgroChem USA, LLC118336116api manufacture, manufacture, analysis, label, pack