Label: A L LAB IODIP 10 - iodine liquid 

  • NDC Code(s): 50138-165-01, 50138-165-02, 50138-165-03, 50138-165-04, view more
    50138-165-05, 50138-165-06, 50138-165-07, 50138-165-08
  • Packager: EXL Laboratories, LLC
  • 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 11/13

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

  • Directions Contents

    1% IODINE POST-MILKING TEAT DIP OR SPRAY

    When used as directed, this product effectively aids in reducing the spread of mastitis.

    DIRECTIONS FOR USE: POST DIPPING:      As soon as possible after removal of milking unit, apply teat dip with either a dip cup or sprayer completely covering the entire teat with the teat dip solution.
    CONTENTS:
    Active Ingredient …………………… 1% Titratable Iodine
    Contains 10% emollients
    DO NOT DILUTE TEAT DIP __ USE AT FULL STRENGTH. IF TEAT DIP BECOMES CLOUDY OR DIRTY IN APPEARANCE, DISCARD AND REPLACE WITH FRESH DIP. DO NOT RETURN CONTAMINATED DIP TO ITS ORIGINAL CONTAINER. If frozen, thaw completely and mix well before using.

    Close
  • Caution First Aid

    CAUTION
    KEEP OUT OF THE REACH OF CHILDREN

    Contains materials which may cause eye damage. May be harmful or fatal if swallowed. Individuals with sensitive skin may experience skin irritation. Protect eyes and skin when handling. Do not take internally. Avoid breathing vapors. Do not mix with any other chemical products. Refer to Material Safety Data Sheet (MSDS).

    FIRST AID:
    If in Eyes:
    Flush with large volumes of water for at least 15 minutes. Call a physician immediately.
    If Swallowed: DO NOT induce vomiting. Rinse mouth promptly then give small amount/glass of milk or water (4 – 6 oz. child/ 10 – 12 oz. adult) (120 – 180 ml child/ 300 – 360 ml adult).  Avoid alcohol. Call a physician immediately. DO NOT give anything by mouth to an unconscious or convulsing person.
    If on Skin: While removing contaminated clothing and shoes, flush with large volumes of water for at least 15 minutes. If irritation develops and persists, get medical attention.
    Inhalation of Vapors: If breathing is difficult or irritation occurs, remove to fresh air. If symptoms persist, get medical attention.
    TOLL FREE EMERGENCY NUMBER: 1-800-424-9300

    Close
  • Product Label

    A and L
    Laboratories

    IODIP 10™

    Part # 852165

    Manufactured by:
    EXL Laboratories, LLC.  1001 Glenwood Ave,  Minneapolis, MN 55405
    Net Contents: 15 GALLONS (56.8 L)  Lot # 00010312A  Expires: 10/2013

    EXLLab IODIP 10 Label

    Close
  • INGREDIENTS AND APPEARANCE
    A L LAB IODIP 10 
    iodine liquid
    Product Information
    Product Type OTC ANIMAL DRUG LABEL Item Code (Source) NDC:50138-165
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    IODINE (IODINE) IODINE 10000 mg  in 1 L
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:50138-165-01 9.5 L in 1 JUG
    2 NDC:50138-165-02 19 L in 1 JUG
    3 NDC:50138-165-03 56.8 L in 1 DRUM
    4 NDC:50138-165-04 114 L in 1 DRUM
    5 NDC:50138-165-05 208.2 L in 1 DRUM
    6 NDC:50138-165-06 946 L in 1 DRUM
    7 NDC:50138-165-07 1003 L in 1 DRUM
    8 NDC:50138-165-08 1040 L in 1 DRUM
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved drug other 11/01/2000
    Labeler - EXL Laboratories, LLC (927483458)
    Registrant - EXL Laboratories, LLC (927483458)
    Establishment
    Name Address ID/FEI Business Operations
    EXL Laboratories, LLC 927483458 api manufacture, manufacture
    Close