Label: AL LAB IODIP 15 - iodine liquid

  • NDC Code(s): 50138-015-01, 50138-015-02, 50138-015-03, 50138-015-04, view more
    50138-015-05, 50138-015-06, 50138-015-07, 50138-015-08
  • 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 09/13

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

  • Directions Contents

    1.0% IODINE PRE-AND POST MILKING TEAT DIP OR SPRAY

    DIRECTIONS FOR USE:

    PRE-DIPPING: 1. Remove excessive soils from teats prior to application of the teat dip solution. 2. Forestrip milk from each quarter for mastitis detections and to initiate milk let-down. (This procedure may be implemented after application of the teat dip  as outlined in step 3.) 3. Apply teat dip with either a teat cup or sprayer completely covering the entire teat with the teat dip solution. Allow 20-40 seconds contact time. 4. Wipe each teat with a single service towel removing all dip and soil from the teat surface. 5. Attach milking unit:

    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.

    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.

    CONTENTS:

    Active Ingredient:.........1.0% Titratable Iodine

    Contains 5% emollients

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  • 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

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  • Product Label

    A and L
    Laboratories

    IODIP 15™

    Control: 00008213A

    Manufactured by:
    EXL Laboratories, LLC.  1001 Glenwood Ave,  Minneapolis, MN 55405

    Net Contents: 55 Gals.  (208 L)    275 Gals.   (1041 L)   

    Lot #:                    Control: 00008213A       Expires:

    EXLLAB AL IODIP15 015 Label

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  • INGREDIENTS AND APPEARANCE
    AL LAB IODIP 15 
    iodine liquid
    Product Information
    Product Type OTC ANIMAL DRUG LABEL Item Code (Source) NDC:50138-015
    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:50138-015-01 9.5 L in 1 JUG
    2 NDC:50138-015-02 19 L in 1 JUG
    3 NDC:50138-015-03 56.8 L in 1 DRUM
    4 NDC:50138-015-04 114 L in 1 DRUM
    5 NDC:50138-015-05 208.2 L in 1 DRUM
    6 NDC:50138-015-06 946 L in 1 DRUM
    7 NDC:50138-015-07 1003 L in 1 DRUM
    8 NDC:50138-015-08 1041 L in 1 DRUM
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved drug other 08/01/2013
    Labeler - EXL Laboratories, LLC (927483458)
    Registrant - EXL Laboratories, LLC (927483458)
    Establishment
    Name Address ID/FEI Business Operations
    EXL Laboratories, LLC 927483458 api manufacture, manufacture
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