Label: FULL-DINE- iodine solution

  • NDC Code(s): 62897-720-01, 62897-720-05, 62897-720-15, 62897-720-55, view more
    62897-720-75
  • Packager: Brown Dairy Equipment
  • Category: OTC ANIMAL DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

NOTE: Most over the counter (OTC) are not reviewed and approved by the FDA. However, they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated 01/13

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  • SPL UNCLASSIFIED SECTION

    BROWN DAIRY EQUIP.

    FULL-DINE

    Premium Sanitizing Teat Dip

    ACTIVE INGREDIENT: 1% Active Iodine Contains 10% Glycerine

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  • DIRECTIONS FOR USE

    DIRECTIONS FOR PRE-DIPPING

    1. Remove excessive organic soils from teats prior to the application of teat dip solution.
    2. Forestrip milk from each quarter for mastitis detection and to initiate milk “let down”. (This procedure may be implemented after application of pre-dip as outlined in Step 3.)
    3. Apply FULLDUAL-DINE with either a dip cup or a sprayer completely covering the entire teat with the teat dip solution. Allow 15-45 seconds of contact time.
    4. Wipe each teat with a single service towel removing all dip and soil from teat surface.
    5. Attach milking unit.

    DIRECTIONS FOR POST DPPING

    1. After removal of milking unit, apply FULL-DINE with either a dip cup or sprayer completely covering the entire teat with the teat dip solution.

    Do not dilute teat dip – Use at full strength. If teat dip becomes cloudy or dirty, discard and replace with fresh dip. Do not return contaminated dip to original container.

    If frozen, thaw completely and mix well before using.

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  • PRECAUTIONARY STATEMENTS

    DANGER - KEEP OUT OF REACH OF CHILDREN - CAN CAUSE EYE DAMAGE

    Protect eyes when handling. DO NOT get in eyes or on clothing. Harmful is swallowed. Avoid contamination of food.

    FIRST AID

    Eyes: In case of contact with eyes, flush immediately with plenty of water for at least 15 minutes. Call a physician.

    Internal: If swallowed, promptly rinse mouth with water then give a large quantity of milk or water. Avoid alcohol. Contact a physician immediately. Never give anything by mouth to an unconscious person.

    FOR ASSISTANCE WITH MEDICAL EMERGENCY, CALL 1-800-367-5178.

    REFER TO MATERIAL DATA SAFETY SHEET.

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  • PRINCIPAL DISPLAY PANEL/REPRESENTATIVE LABEL
  • INGREDIENTS AND APPEARANCE
    FULL-DINE 
    iodine solution
    Product Information
    Product Type OTC ANIMAL DRUG LABEL Item Code (Source) NDC:62897-720
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    IODINE (IODINE) IODINE 10 g  in 1 L
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:62897-720-01 3.8 L in 1 BOTTLE
    2 NDC:62897-720-05 18.9 L in 1 DRUM
    3 NDC:62897-720-15 56.8 L in 1 DRUM
    4 NDC:62897-720-55 208.2 L in 1 DRUM
    5 NDC:62897-720-75 1041 L in 1 TANK
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved drug other 09/18/2002
    Labeler - Brown Dairy Equipment (017030149)
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