Label: HB ZINC SUPREME- zinc footbath solution

  • NDC Code(s): 64892-024-16, 64892-024-17, 64892-024-18, 64892-024-21, view more
    64892-024-88
  • Packager: Wausau Chemical
  • 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 January 7, 2020

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

  • DISPOSAL AND WASTE HANDLING

    Dispose of contents/container to an approved waste disposal plant.

  • ENVIRONMENTAL WARNING

    Very toxic to aquatic life with long lasting effects. Avoid release to the environment. Collect spillage.

  • GENERAL PRECAUTIONS

    DANGER / Keep Out of Reach of Children

  • First Aid:

    IF SWALLOWED: Call a POISON CENTER or doctor/ physician if you feel unwell.
    IF SWALLOWED: Rinse mouth. Do NOT induce vomiting.
    IF ON SKIN (or hair): Remove/ Take off immediately all contaminated clothing. Rinse skin with water/ shower.
    IF INHALED: Remove victim to fresh air and keep at rest in a position comfortable for breathing. Immediately call a POISON CENTER or doctor/ physician.
    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 or doctor/ physician.

  • SAFE HANDLING WARNING

    Do not breathe fume/ gas/ mist/ vapors/ spray. Wash skin thoroughly after handling. Do not eat, drink or smoke when using this product. Wear protective gloves/ protective clothing/ eye protection/ face protection. Wash contaminated clothing before reuse.

  • STORAGE AND HANDLING

    Store locked up. Store in a corrosive resistant container. Keep only in original container. Absorb spillage to prevent material-damage.
    Store above 32 °F (0 °C). If frozen, thaw and mix back into solution. Product quality will not be affected.

  • VETERINARY INDICATIONS

    DIRECTIONS:
    Mix 3-5 gallons of HB Zinc Supreme with 50 gallons of clean, warm water to create final solution for use in footbaths for cattle.

    For best results:
    Cattle hooves need to be clean prior to walking through the footbath solution to allow complete and effective contact with the hoof. If conditions exist that cause hooves to be dirty a prewash or rinse bath with Hoof Bath Detergent hoof cleaner conditioner should be used in front of the treatment footbath.

    Solution should be changed after 200 cow passes.

    Use in conjunction with a total hoof care program including proper hoof trimming, attention to cow comfort and sanitation, correct nutrition and proper footbath management.

    Footbath treatments are recommended every other day at a minimum as a good management practice for maintaining healthy hooves.

     It is recommended that you switch out active footbath treatment every several weeks to avoid overuse of a single active ingredient.

  • PRINCIPAL DISPLAY PANEL

    Active Ingredient – zinc sulfate monohydrate......................................................................25.4%

    Wausau Chemical Corporation

    2001 N River Drive

    Wausau, WI 54403

    800-950-6656

    Representative label

  • INGREDIENTS AND APPEARANCE
    HB ZINC SUPREME 
    zinc footbath solution
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:64892-024
    Route of AdministrationTopical
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC SULFATE MONOHYDRATE (UNII: PTX099XSF1) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION339.1 g  in 1 L
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:64892-024-1618.9 L in 1 PAIL
    2NDC:64892-024-1756.78 L in 1 DRUM
    3NDC:64892-024-18113.6 L in 1 DRUM
    4NDC:64892-024-21208.2 L in 1 DRUM
    5NDC:64892-024-881040 L in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other01/07/2020
    Labeler - Wausau Chemical (006136220)
    Registrant - Wausau Chemical (006136220)
    Establishment
    NameAddressID/FEIBusiness Operations
    Wausau Chemical006136220manufacture, api manufacture