Label: UDDERCARE PLUS PART B- stabilized sodium salt of chlorous acid solution
- NDC Code(s): 46066-414-17, 46066-414-21
- Packager: Aspen Veterinary Resources
- Category: OTC ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: 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 Information
Updated July 8, 2019
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- SAFE HANDLING WARNING
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VETERINARY INDICATIONS
DIRECTIONS:
IMPORTANT: Do not mix Uddercare+ Part B with water, or any other products unless specified in the product use instructions. If transferred from this container to any other, make sure that the other container is thoroughly pre-cleaned and bears the proper container labeling for Uddercare+ Part B.
If product in dip cup becomes visibly dirty, discard contents and replenish with undiluted product. Do not reuse or return any unused product to the original container.
Mix Directions: Measure equal volumes of Uddercare+ Part A and Uddercare+ Part B into clean containers. Mix until uniform in color. Mix only the quantity needed for one milking shift and discard the remainder.
Pre-Milk Dipping: Fill teat dip cup with properly mixed Uddercare+ Part A and Uddercare+ Part B. Before each cow is milked, dip each teat full-length into the teat dip cup containing the product. Wipe teats dry after dipping using single-service towels to avoid contamination of milk.
Post-Milk Dipping: Immediately after each milking, use mixed Uddercare+ Part A and Uddercare+ Part B at full strength. Dip each teat full-length into the teat dip cup containing mixed product. Allow to air dry. Do not wipe. Always use fresh full strength, mixed product. Do not turn cows out in freezing weather until product is completely dry.
PRECAUTION: Uddercare+ Part B is not intended to cure or help the healing of chapped or irritated teats. As with any germicide, irritation or sensitization may occur in sensitive animals. In case of teat irritation or chapping, have the condition examined and, if necessary, treated by a veterinarian.
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OTHER SAFETY INFORMATION
FIRST AID
IN CASE OF EYE CONTACT: Rinse immediately with plenty of water, also under the eyelids, for at least 15 minutes. Remove contact lenses, if present and easy to do. Continue rinsing. Get medical attention immediately.
IN CASE OF SKIN CONTACT: Wash off immediately with plenty of water for at least 15 minutes. Use a mild soap if available. Wash clothing before reuse. Thoroughly clean shoes before reuse. Get medical attention immediately.
IF SWALLOWED: Rinse mouth with water. Do NOT induce vomiting. Never give anything by mouth to an unconscious person. Get medical attention immediately.
IF INHALED: Remove to fresh air. Treat symptomatically. Get medical attention if symptoms occur.
READ SAFETY DATA SHEET (SDS) BEFORE USING THIS PRODUCT
EMERGENCY HEALTH INFORMATION: Contact local poison control. -
PRINCIPAL DISPLAY PANEL
aspen DIARY SOLUTIONS
UDDERCARE+ PART B
ACTIVE INGREDIENT:
Stabilized Sodium Salt of Chlorous Acid................................0.54%
INERT INGREDIENTS:...................................................... 99.46%
TOTAL:..............................................................................100.00%
Sanitizing Pre/Post Teat Dip
Uddercare+ Part B is formulated to be used as a companion product for Uddercare+ Part A.
An aid in reducing the spread of organisms which may cause mastitis
NET CONTENTS: 208 L (55 US GAL)
6301575
Manufactured for:
Aspen Veterinary Resources®, Ltd.
3155 Heartland Drive, Liberty, MO 64068
1-800-203-5620 761372/5300/0315
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INGREDIENTS AND APPEARANCE
UDDERCARE PLUS PART B
stabilized sodium salt of chlorous acid solutionProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:46066-414 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM CHLORITE (UNII: G538EBV4VF) (CHLORITE ION - UNII:Z63H374SB6) SODIUM CHLORITE 5.4 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:46066-414-17 56800 mL in 1 DRUM 2 NDC:46066-414-21 208000 mL in 1 DRUM Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 02/12/2015 Labeler - Aspen Veterinary Resources (627265361)