Label: PRO-SAN LV BASE- sodium chlorite solution

  • NDC Code(s): 29983-0105-4, 29983-0105-6, 29983-0105-8, 29983-0105-9
  • Packager: IBA
  • 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 March 20, 2023

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  • ACTIVE INGREDIENT

    SODIUM CHLORITE...........0.70%

  • INDICATIONS AND USAGE

    MIXING DIRECTIONS: TO MAKE A READY-TO-USE SOLUTION OF PRO-SAN LV TEAT DIP, ADD EQUAL VOLUMES OF PRO-SAN LV BASE AND PRO-SAN LV ACTIVATOR INTO A CLEAN DIP CUP/CONTAINER AND MIX UNTIL THE COLOR IS UNIFORAM THROUGHOUT. DO NOT DILUET. DO NOT MIX WITH ANY OTHER PRODUCTS. DISCARD ANY UNUSED TEAT DIP. UNUSED TEAT DIP MAY BE DILUTED WITH WATER AND SAFELY FLUSHED DOWN THE DRAIN. 

    1. Use teat dip applicators made of plastic or other non-corrosive materials. Do not use cups made of aluminum.
    2. When solution in the teat dip cup becomes dirty and/or noticeably loses color, discard remaining contents and refill cup with fresh teat dip.
    3. Do not use this product for cleaning or sanitizing equipment
    4. Wash Teat Dip cups after each milking.
    RECOMMENDED PROCEDURES FOR TEAT SANITATION
    A. PRE-MILKING (PRE-DIPPING)
    1. REMOVE VISIBLE SOILS FROM THE TEATS.
    2. OBSERVE FOREMILK BY STRIPPING TWO OR THREE STREAMS OF MILK INTO A STRIP CUP.
    3. DIP OR SPRAY THE COW'S TEATS FULL LENGTH WITH READY-TO-USE PRO-SAN LV TEAT DIP.
    4 WAIT APPROXIMATELY 15-30 SECONDS.
    5. REMOVE ALL TEAT DIP BY THOROUGHLY DRYING THE TEATS AND TEAT ORIFICES AND UDDER (IF SPRAYING), WITH A CLEAN, SINGLE SERVICE PAPER TOWEL(S).
    6. ATTACH MILKING UNIT
    B. POST-MILKING (POST DIPPING)
    Immediately after milking dip or spray all teats full length with READY-TO-USE PRO-SAN LV TEAT DIP. Ensure good coverage of all sides of the teats and teat orifices. Allow to dry. Do not wipe. Do not turn cows out in freezing weather until teat dip is completely dry.

  • WARNING

    DO NOT DILUTE THIS PRODUCT
    DO NOT RETURN TEAT DIP LEFT IN THE TEAT DIPPER TO STORAGE CONTAINER
    ENSURE THAT DIPPED TEATS ARE DRY BEFORE EXPOSING THE ANIMALS TO WEATHER CONDITIONS WHICH MAY CAUSE DAMAGE TO THE TEATS.

    STORE AT ROOM TEPERATURE. ALWAYS STORE AWAY FROM DIRECT SUNLIGHT.

    PROTECT THIS PRODUCT FROM FREEZING. HOWEVER, FREEZING WILL NOT AFFECT PRO-SAN LV PROVIDED THAT THE CONTENTS ARE THAWED COMPLETELY AND AGITATED THOROUGHLY BEFORE MIXING BASE AND ACTIVATOR TOGETHER.

    CAUTION: KEEP OUT OF REACH OF CHILDREN.
    AVOID CONTACT WITH FOOD. DO NOT TAKE INTERNALLY.

  • FIRST AID PROCEDURES

    EYE CONTACT: ARINSE CAUSTIOUSLY WITH FRESH,TEPID WATER FOR SEVERAL MINUTES.REMOVE CONTACT LENSES IF PRESENT AND EASY TO DO. CONTINUE RINSING FOR 15 MINUTES. GET IMMEDIATE MEDICAL ADVICE/ATTENTION.

    SKIN CONTACT: FOR READY-TO-USE PRODUCTS, WASH ANY SENSITIVE AREAS.

    INGESTION: DO NOT INDUCE VOMITING.NEVER GIVE ANYTHING BY MOUTH TO AN UNCONSCIOUS PERSON.DRINK LARGE AMOUNTS OF WATER. IF VOMITING OCCURS, KEEP AIRWAYS OPEN. KEEP HEAD LAWER THAN THE HIPS TO PREVENT ASPIRATION INTO THE LUNGS. GET IMMEDIATE MEDICAL ADVISE/ATTENTION.

    ALWAYS SEEK IMMEDIATE MEDICAL ATTENTION

    FOR MEDICAL EMERGENCIES CALL 1-800-424-9300

  • PRO-SAN LV BASE

    PRO-SAN LV BASE

  • INGREDIENTS AND APPEARANCE
    PRO-SAN LV BASE 
    sodium chlorite solution
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:29983-0105
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM CHLORITE (UNII: G538EBV4VF) (CHLORITE ION - UNII:Z63H374SB6) SODIUM CHLORITE8.9 g  in 1 L
    Product Characteristics
    Colorwhite (CLEAR) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:29983-0105-418.9 L in 1 DRUM
    2NDC:29983-0105-656.7 L in 1 DRUM
    3NDC:29983-0105-8207.9 L in 1 DRUM
    4NDC:29983-0105-91039.5 L in 1 DRUM
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other02/28/2023
    Labeler - IBA (019494160)