Label: AL LAB IODIP 15 - iodine liquid
view more50138-015-05, 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
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- 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.
Active Ingredient:.........1.0% Titratable Iodine
Contains 5% emollientsClose
- Caution First Aid
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).
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: 1-800-424-9300Close
- Product Label
A and L
EXL Laboratories, LLC. 1001 Glenwood Ave, Minneapolis, MN 55405
Net Contents: 55 Gals. (208 L) 275 Gals. (1041 L)
Lot #: Control: 00008213A Expires:
- INGREDIENTS AND APPEARANCE
AL LAB IODIP 15
Product Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:50138-015 Route of Administration TOPICAL DEA Schedule Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4) 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