Label: ASPEN SUPERIOR - iodine liquid
view more50138-171-05, 50138-171-06, 50138-171-07, 50138-171-08
- 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.
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- Usage Directions Active Ingredients
PRE-DIPPING/SPRAYING: Teats should be clean and dry before dipping. Dip/spray with undiluted product and allow to dry 30-60 seconds contact time. Wipe the teats dry.
POST -DIPPING/SPRAYING: Dip/spray teats with undiluted product after milking. Allow to air dry. With freshening cows, begin dipping teats twice daily for about 10 days before calving. For dry cows, dip/spray teats once a day for 3-4 days following the last milking.
DURING COLD WEATHER do not turn cows out until teats are dry.
UDDER WASH: To avoid contamination of milk, wash teats with this product diluted at 1oz. (30mL) per 1-2 gallon (4-8L) of lukewarm water. Then dry each cow's udder and teats with clean towels before milking.
DO NOT USE THIS PRODUCT FOR CLEANING AND/OR SANITIZING EQUIPMENT
IMPORTANT: TEAT IRRITATION OR CHAPPING: Teat dips have the potential to cause irritation or chapping. If you observe abnormal irritation or chapping, call 1-800-225-3832 or contact your dealer.
ACTIVE INGREDIENTS: Nonylphenolyethoxy (12 moles EO) ethanol-iodine complex providing 0.5% titratable iodine (5,000 mg/L)
Contains 6% skin conditioners
- Caution Storage and Disposal
KEEP OUT OF REACH OF CHILDREN
HARMFUL IF SWALLOWED - HARMFUL IF INHALED - CAUSES EYE IRRITATION
SEE BELOW FOR ADDITIONAL PRECAUTIONS OR CONTACT MSDS SHEET
TOLL FREE EMERGENCY NUMBER: 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.
EXTERNAL: in case of contact, immediately flush contaminated skin with plenty of water. If irritation occurs and persists, call a physician.
INTERNALLY: If conscious, dilute by giving several glasses of water or milk. Do not induce vomiting. If vomiting does occur, repeat giving glasses of water or milk. Give prompt medical attention. NEVER GIVE ANYTHING BY MOUTH 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 small spill (less than one gallon), flood area with 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
Aspen Dairy Solutions
QUALITY MILK CONTROL
0.5% IODINE PRE AND POST-MILKING TEAT DIP OR SPRAY
Net Contents: 15 GALLONS (56.8 L)
Lot # 00010252A Expires: 10/2014
EXL Laboratories, LLC
1001 Glenwood Ave.
Minneapolis, MN 55405
- INGREDIENTS AND APPEARANCE
Product Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:50138-171 Route of Administration TOPICAL DEA Schedule Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4) IODINE 5000 mg in 1 L Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50138-171-01 9.5 L in 1 JUG 2 NDC:50138-171-02 19 L in 1 JUG 3 NDC:50138-171-03 56.8 L in 1 DRUM 4 NDC:50138-171-04 114 L in 1 DRUM 5 NDC:50138-171-05 208 L in 1 DRUM 6 NDC:50138-171-06 946 L in 1 DRUM 7 NDC:50138-171-07 1003 L in 1 DRUM 8 NDC:50138-171-08 1041 L in 1 DRUM Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 09/01/2008 Labeler - EXL Laboratories, LLC (927483458) Registrant - EXL Laboratories, LLC (927483458) Establishment Name Address ID/FEI Business Operations EXL Laboratories, LLC 927483458 api manufacture, manufacture