Label: 4XLA BASE- sodium chlorite solution

  • NDC Code(s): 47593-607-16, 47593-607-17, 47593-607-21, 47593-607-44
  • Packager: Ecolab Inc.
  • 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 July 9, 2019

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

  • SAFE HANDLING WARNING

    FOR USE ONLY WITH 4XLA® ACTIVATOR

    DANGER: Causes severe skin burns and eye damage. Wash skin thoroughly after handling. Wear protective gloves/ protective clothing/ eye protection/ face protection.

    DISPOSAL: Unused teat dip may be diluted with water and flushed down drain. Do not reuse containers. Empty containers should be thoroughly rinsed with water and taken to a recycling center.

    KEEP OUT OF THE REACH OF CHILDREN

    NOT FOR HUMAN USE

    AVOID FREEZING: If product is exposed to freezing temperatures, components must be mixed thoroughly prior to use.

  • VETERINARY INDICATIONS

    DIRECTIONS FOR USE: Measure equal volumes of 4XLA® base and 4XLA activator into a clean dip cup/container and mix until the color is uniform through-out. Do not dilute. Mix only enough product for one milking of the herd. Dip cups should be washed after each milking.

    APPLICATION:

    Pre-Milking: If teats are visibly dirty, wash and dry teats with a single service towel prior to dipping. Before each cow is milked, dip the teats as far up as possible. Leave 4XLA Teat Dip on teats for at least 15-30 seconds. Wipe teats dry using a single service towel before milking.

    Post-Milking: Immediately after milking, dip teats at least 2/3 to all their length in 4XLA Teat Dip. Allow to air dry. DO NOT WIPE. 4XLA Teat Dip can be used as a post-dip alone, or as a pre- and post-milking teat dip.

    Always use freshly mixed, full strength 4XLA Teat Dip. If product in dip cup becomes visibly dirty, discard contents and fill with fresh 4XLA Teat Dip.

    Note 1: If teat irritation occurs, discontinue use until irritation subsides. Consult your veterinarian and milking equipment service personnel if irritation persists.

    Note 2: The gold color in the mixed product fades with time. At higher temperatures the fading is more rapid. However, this will not affect the efficacy of the product.

    Note 3: 4XLA should be used only with a compatible pre-dip or udder wash.

  • OTHER SAFETY INFORMATION

    IF SWALLOWED: Rinse mouth. Do NOT induce vomiting. IF ON SKIN (or hair): Take off immediately all contaminated clothing. Rinse skin with water/ shower. IF INHALED: Remove person to fresh air and keep comfortable for breathing. Immediately call a POISON CENTER/ doctor. IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. Immediately call a POISON CENTER/ doctor. Wash contaminated clothing before reuse.

  • PRINCIPAL DISPLAY PANEL

    SELECT SIRES

    6301916

    4XLA®

    GERMICIDAL PRE- & POST-MILKING TEAT DIP

    An aid in reducing the spread of organisms which may cause mastitis

    BASE

    ACTIVE INGREDIENT:

    Sodium Chlorite................................................... 0.6%

    INERT INGREDIENTS:....................................... 99.4%

    TOTAL:.............................................................. 100.0%

    208 L (55 US GAL)

    4XLA® is a registered trademark of

    Ecolab Inc., St. Paul, MN 55102

    Made in USA

    U.S. Patent RE37263, U.S. Patent 5,384,134

    Foreign Patents Issued and Pending

    Distributed by:

    Select Sires, Inc.

    11740 U.S. 42N P.O. Box 143 Plain City, OH  43064-0143

    614-873-4683

    www.selectsires.com

    representative label

  • INGREDIENTS AND APPEARANCE
    4XLA BASE 
    sodium chlorite solution
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:47593-607
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM CHLORITE (UNII: G538EBV4VF) (CHLORITE ION - UNII:Z63H374SB6) SODIUM CHLORITE6 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:47593-607-1618900 mL in 1 PAIL
    2NDC:47593-607-1756800 mL in 1 DRUM
    3NDC:47593-607-21208000 mL in 1 DRUM
    4NDC:47593-607-441134000 mL in 1 CONTAINER
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other05/08/2014
    Labeler - Ecolab Inc. (006154611)
    Establishment
    NameAddressID/FEIBusiness Operations
    Ecolab Inc.943879395manufacture, analysis, label, relabel, pack, api manufacture