Your browser does not support JavaScript! UDDERLY SOFT (IODINE) LIQUID [EXL LABORATORIES, LLC]

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RxNorm Names

UDDERLY SOFT (iodine) liquid
[EXL Laboratories, LLC]


Category DEA Schedule Marketing Status
OTC ANIMAL DRUG LABEL unapproved drug other
NOTE: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 Sections

Usage Directions Teat irritation and chapping Active Ingredient

1 % IODINE POST-MILKING TEAT DIP OR SPRAY

USAGE DIRECTIONS
POST-DIPPING/SPRAYING:

 Dip/spray teats with undiluted product immediately after milking. Allow to air dry. Replace the solution if it becomes visibly dirty. With freshening cows, begin dipping teats twice daily for about 10 days before calving. For dry cows, dip/spray teats once a day for several days following the last milking. During cold weather, do not turn out cows until teats are dry to prevent chapping and freezing. If necessary, wipe dry with a single service towel.
UDDER WASH: To avoid contamination of milk, wash teats with this product diluted at 1 oz. (30 ml) per 2 gallons (8 L) of lukewarm water. Then dry each cow’s udder and teats with individual clean towels.

DO NOT USE THIS PRODUCT FOR CLEANING AND/OR SANITIZING EQUIPMENT.

IMPORTANT: TEAT IRRITATION OR CHAPPING:  Teat dips have the potential to cause irritation of a cow’s teats or milker’s hands individual tolerance to a particular formulation as well as other factors (dry or cold weather, improper teat dip application, bedding quality, milking equipment, etc.) may also affect teat condition. If you observe abnormal irritation or chapping, discontinue and use and call the technical service department at 1-800-225-3832, or contact your dealer.

ACTIVE INGREDIENTS: Nonylphenoxypolyethoxy (12 moles EO) ethanol-iodine complex providing 1.0% titratable iodine (10.000 mg/L)
Contains 10% skin conditioners.

Caution First Aid Storage-Spillage

CAUTION – KEEP OUT OF THE REACH OF CHILDREN
HARMFUL IF SWALLOWED – HARMFUL IF INHALED – CAUSES EYE IRRITATION
SEE BELOW INFORMATION FOR ADDITIONAL PRECAUTIONS AND/OR CONSULT MATERIAL SAFETY DATA SHEET

Personnel familiar with this product are available 24 hours a day, 7 days a week.

FOR EMERGENCIES CALL 1-800-424-9300
PRECAUTIONS:

 Protect eyes from contact with this product. Keep container tightly closed when not in use. Use with adequate ventilation. Wash thoroughly after handling product.
FIRST AID:
EXTERNAL:
In case of contact, immediately flush contaminated skin with plenty of water. If irritation occurs and persists, call a physician.
INTERNAL: If conscious, dilute by giving several glasses of water or milk. Do not induce vomiting. If vomiting does occur, repeat giving several glasses of water or milk. Get prompt medical attention. NEVER GIVE ANYTHING BY MOUYH TO AN UNCONSCIOUS PERSON.
EYES: Immediately flush with plenty of clean, running water for at least 15 minutes, holding eyelids apart to ensure flushing of the entire eye surface. If irritation persists, call a physician.
STORAGE AND   DISPOSAL: Store this product in a cool, dry area away from direct sunlight and heat to avoid deterioration. Store in a locked cabinet or room to keep it out of the reach of children. Dispose of according to Federal, State, and local laws.
SPILLAGE: In case of a small spill (less than one gallon) flood area with a large quantity of water. For larger spills, contain and remove with inert absorbent and dispose of according to Federal, State, and local laws.
KEEP FROM FREEZING.

Product Label

LITTLE ROCK
COOPERATIVE                                        UDDERLY SOFT  1%
CREAMERY

Manufactured in the U.S.A. by EXL Laboratories, LLC. 
1011  Glenwood Avenue, Minneapolis, MN 55405  Toll free 1-800-225-3832

Part # 20011

Net Contents:  275 GALLONS (1040 L)
Lot #: 00010312A  Expires: 10/2013

EXL Lab Udderly Soft Label

UDDERLY SOFT 
iodine liquid
Product Information
Product TypeOTC ANIMAL DRUG LABELItem Code (Source)NDC:50138-011
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
IODINE (IODINE) IODINE10000 mg  in 1 L
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:50138-011-019.5 L in 1 JUG
2NDC:50138-011-0219 L in 1 JUG
3NDC:50138-011-0356.8 L in 1 DRUM
4NDC:50138-011-04114 L in 1 DRUM
5NDC:50138-011-05208.2 L in 1 DRUM
6NDC:50138-011-06946 L in 1 DRUM
7NDC:50138-011-071003 L in 1 DRUM
8NDC:50138-011-081040 L in 1 DRUM
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other05/01/2006
Labeler - EXL Laboratories, LLC (927483458)
Registrant - EXL Laboratories, LLC (927483458)
Establishment
NameAddressID/FEIBusiness Operations
EXL Laboratories, LLC927483458api manufacture, manufacture

Revised: 11/2013
 
EXL Laboratories, LLC

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