Label: DAIRYLAND BRAND IODINE TEAT DIP CONTROLLED- iodine liquid

  • NDC Code(s): 60282-2201-1, 60282-2201-2, 60282-2201-3, 60282-2201-4
  • Packager: Stearns Packaging Corporation
  • 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 12, 2017

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  • GENERAL PRECAUTIONS

    GREAT FOR FOAMING!

    TEAT DIPPING is an important part of a MASTITIS
    CONTROL PLAN:

    1. Dip teats immediately after milking.
    2. Use good milking and environmental management
        procedures.
    3. Use properly functioning milking equipment.
    4. Treat every quarter of every cow at dry off.
    5. Identify and treat or manage clinical cases promptly.
    6. Cull chronically infected cows.

    TEAT DIPPING IN COLD WEATHER:
    When the temperature falls below 10 degrees F, or when wind chill is significant, special
    precautions should be taken to avoid chapped and frozen teats.

    1. Teats should be dry before turning cows out into cold weather.
    2. When teats are dipped after milking, allow 30 seconds contact, and blot
        off any excess teat dip with a single service towel.
    3. Warm the teat dip to reduce drying time.
    4. Provide windbreaks in outside areas for cows.
    5. Monitor fresh cows with swollen udders and teats since
        they are more susceptible to chapped and frozen teats.

  • DOSAGE & ADMINISTRATION

    TAKE TIME

    OBSERVE
    LABEL DIRECTIONS

    DIRECTIONS FOR USE:

    • DO NOT DILUTE.
    • Dip teats immediately after milking as a routine part of milking
      procedures.
    • Dip to THOROUGHLY COVER at least the lower one-third of the teat
      (preferably to the base of the udder), IMMEDIATELY after every milking.
  • STORAGE AND HANDLING

    • Empty and clean dip cups after each milking, or during milking, if they
      become contaminated.
    • Do not pour use dip back into original container.
    • KEEP FROM FREEZING
    • Keep container closed to prevent contamination.
    • Store container in an upright position.
  • USER SAFETY WARNINGS

    FIRST-AID
    EYES: If contact with eyes occurs, flush with plenty of cool water for 15
    minutes. Consult a physician.
    INTERNAL: May be harmful if swallowed. If ingested, drink large amounts
    of water or milk. DO NOT induce vomiting. Get medical attention
    immediately.

    FOR ASSISTANCE WITH MEDICAL
    EMERGENCY CONTACT:
    CHEM-TEL, 1-800-255-3924

  • PRINCIPAL DISPLAY PANEL

    DAIRYLAND BRAND

    CONTROLLED
    IODINE TEAT DIP

    SANITIZING TEAT DIP
    An Aid in Reducing the Spread of
    Organisms WhichMay Cause Mastitis

    ACTIVE INGREDIENTS:
    Concentrated Iodophor, containing Nonylphenol, ethoxylated iodine complex.
    (provides 1% titratable iodine, equivalent to 10,000 ppm titratable iodine)

    EMOLLIENT SYSTEM contains 10% glycerin.

    KEEP OUT OF THE REACH OF CHILDREN
    ​CAUTION: HARMFUL IF SWALLOWED / EYE IRRITANT

    STEARNS PACKAGING CORPORATION
    4200 Sycamore Avenue • Madison, WI 53714

    NET CONTENTS: 1 U.S. FL. GALLON (3.78 L)

    DB ITD 1 Image

  • INGREDIENTS AND APPEARANCE
    DAIRYLAND BRAND IODINE TEAT DIP  CONTROLLED
    iodine liquid
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:60282-2201
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4) IODINE10 g  in 1 L
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 100 g  in 1 L
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:60282-2201-13.78 L in 1 BOTTLE, PLASTIC
    2NDC:60282-2201-218.93 L in 1 PAIL
    3NDC:60282-2201-356.78 L in 1 DRUM
    4NDC:60282-2201-4208.2 L in 1 DRUM
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other01/02/1999
    Labeler - Stearns Packaging Corporation (006069256)
    Registrant - Stearns Packaging Corporation (006069256)
    Establishment
    NameAddressID/FEIBusiness Operations
    Stearns Packaging Corporation006069256manufacture, api manufacture