Label: METZ 0.5% FRESH TEAT DIP- iodine solution

  • NDC Code(s): 86067-0021-1, 86067-0021-2
  • Packager: Surpass Chemical Company, 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 December 27, 2022

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

  • DESCRIPTION

    NORTH COUNTRY DAIRY SUPPLY, LLC.                                                                                                               NPE

    METZ 0.5% FRESH TEAT DIP                                                                                                                              FREE

    AIDS IN CONTROLLING THE SPREAD OF BACTERIA THAT MAY CAUSE MASTITIS                                                     PRODUCT #: 630800

  • INSTRUCTIONS FOR USE

    DIRECTIONS:
    PRE-MILKING: Throughly clean all teats. If water or sanitizer is used to clean the teats, be sure to completely dry the teats with a single service paper towel. Forestrip two or three streams Dip the cow's teats full length with Metz Fresh 0.5% Teat Dip. Wait 15-30 seconds. Remove all residues by throughly drying the teats with a clean, single service paper towel. Attach milker unit.
    POST-MILKING: Immediately after milking, dip all teats to the base of the udder with Metz Fresh 0.5% Teat Dip. On dry cows, dip each teat once per day for five days following the last milking.
    GENERAL: Use teat dipping cups made of plastic, rubber, or stainless steel. Do not use cups made of aluminum.

  • GENERAL PRECAUTIONS

    CAUTION:
    Do not take internally. Avoid contact with eyes, skin, clothing, and food. Avoid breathing vapors.
    Always use full strength Teat Dip. Discard solution if it becomes faded or noticeably dirty. Do not use this dip to sanitize
    milking equipment or utensils

  • PRECAUTIONS

    PRECAUTIONARY STATEMENTS
    Prevention: Do not breathe dust/fume/gas/mist/vapors/spray Wash face, hands and any exposed skin thoroughly after
    handling Do not eat, drink or smoke when using this product
    Response: Get medical advice/attention if you feel unwell
    Disposal: Dispose of contents/container to an approved waste disposal plant

  • OTHER SAFETY INFORMATION

    FIRST AID:
    IF SPLASHED IN EYES:Rinse thoroughly with plenty of water, also under the eyelids. If symptoms persist, call a physician.
    IN CASE OF CONTACT: Wash with soap and water.
    IF INHALED: Remove to fresh air.
    IF SWALLOWED: Rinse mouth immediately and drink plenty of water. Never give anything by mouth to an unconscious person.

  • ACTIVE INGREDIENT

    INGREDIENTS:
    ACTIVE: Iodine complex (Provides 1% titratable iodine. Equivalent
    to 10,000 ppm).

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN!

  • SPL UNCLASSIFIED SECTION

                            Surpass Chemical Company, Inc.
                                 www.surpasschemical.com                                                                  24 HOUR EMERGENCY ASSISTANCE:
    Phone: (518) 434-8101                                 1254 Broadway                                                  CHEMTREC 1-800-424-9300
    Fax: (518) 434-2798                                      Albany NY, 12204
    Email: customerservice@surpasschemical.com

  • SPL UNCLASSIFIED SECTION

    BEFORE USING THIS MATERIAL, READ AND
    UNDERSTAND THE CURRENT SAFETY DATA SHEET.

  • PRINCIPAL DISPLAY PANEL

    15GL > container4x1 &1GL container

  • INGREDIENTS AND APPEARANCE
    METZ 0.5% FRESH TEAT DIP 
    iodine solution
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:86067-0021
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4) IODINE0.0275 g  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R) 0.8787 g  in 1 g
    C9-11 PARETH-8 (UNII: 80E6PSE1XL) 0.0354 g  in 1 g
    GLYCERIN (UNII: PDC6A3C0OX) 0.05 g  in 1 g
    LAURETH-11 CARBOXYLIC ACID (UNII: CK7N38KKFK) 0.0033 g  in 1 g
    SODIUM HYDROXIDE (UNII: 55X04QC32I) 0.0021 g  in 1 g
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) 0.003 g  in 1 g
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:86067-0021-1128 g in 1 DRUM
    2NDC:86067-0021-2470 g in 1 DRUM
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other06/10/2016
    Labeler - Surpass Chemical Company, Inc. (002075133)
    Establishment
    NameAddressID/FEIBusiness Operations
    Surpass Chemical Company, Inc.002075133manufacture, api manufacture