Label: CHLORSAN CONCENTRATE TEAT SCRUBBER PART B- sodium chlorite solution

  • NDC Code(s): 17307-3654-1, 17307-3654-2, 17307-3654-3, 17307-3654-4
  • Packager: AgroChem 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 October 31, 2013

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

  • DESCRIPTION

    CHLORINE DIOXIDE / BASE - MUST BE DILUTED PRIOR TO USE (1:4)

  • WARNINGS AND PRECAUTIONS

    FIRST AID:

    1. Immediately flush skin or eyes with

     plenty of water.

    2. Remove contaminated clothing.

    3. SEEK MEDICAL ATTENTION.

    CAUTION:

    * Wear protective equipment when handling.

    * Avoid contact with eyes, skin, and clothing.

    * Avoid inhaling mist or vapors.

    * Keep container closed when not in use.

    * Wash exposed areas thoroughly after handling.

    * Store in original vented container.

    * Do not attempt to return unused material to

     container.

  • ACTIVE INGREDIENT

    INGREDIENTS WHEN MIXED AS DIRECTED:

    Sodium Chlorite - 2.56 %

    Glycerine - 2.0 %

  • INSTRUCTIONS FOR USE

    NOTE: CONCENTRATE - MUST BE

    DILUTED PRIOR TO USE. MIX

    ONE PART CONCENTRATE WITH

    FOUR PARTS WATER BY

    VOLUME.

    DIRECTIONS:

    1. CREATES CHLORINE DIOXIDE. After

    diluting concentrate, mix equal parts of

    Part A and Part B. Reaches minimum

    Chlorine Dioxide levels (150 - 400 ppm)

    within 15 minutes of mixing. Will

    continue to generate minimum Chlorine

    Dioxide levels for up to 24 hours, however

    it is recommended to replace with

    freshly mixed Chlorsan solution sooner.

  • PRINCIPAL DISPLAY PANEL

    image description

  • INGREDIENTS AND APPEARANCE
    CHLORSAN CONCENTRATE TEAT SCRUBBER PART B 
    sodium chlorite solution
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:17307-3654
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM CHLORITE (UNII: G538EBV4VF) (CHLORITE ION - UNII:Z63H374SB6) SODIUM CHLORITE0.0256 kg  in 1 kg
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.02 kg  in 1 kg
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:17307-3654-119 kg in 1 CONTAINER
    2NDC:17307-3654-257 kg in 1 DRUM
    3NDC:17307-3654-3208 kg in 1 DRUM
    4NDC:17307-3654-41040 kg in 1 CONTAINER
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other10/01/2013
    Labeler - AgroChem Inc (805427700)
    Establishment
    NameAddressID/FEIBusiness Operations
    AgroChem Inc805427700api manufacture, manufacture