Label: UDDERGOLD DRY- polyvinylpyrrolidone solution
- NDC Code(s): 47593-852-22, 47593-852-32
- Packager: Ecolab Inc.
- 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 January 24, 2024
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- WARNINGS AND PRECAUTIONS
- INSTRUCTIONS FOR USE
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DOSAGE & ADMINISTRATION
Directions For Use
Use in a well-ventilated area. Do not pour unused product back into the original container. Keep container tightly closed when not in
use. Apply with a disposable 3 fl oz paper cup.
At Dry Off
At last milking prior to dry off, milk out cow completely. Infuse dry cow product into clean, dry teat, according to product label
instructions. Dip the entire length of the teat in UDDERgold® Dry Teat Dip. For maximum protection, a second application may be
applied after the first coating is dry.
10 Days Prior to Calving
Clean teat thoroughly and wipe with dry towel. Dip entire length of teat in to UDDERgold® Dry Teat Dip. Dip should remain on teat
for 3-7 days. Observe daily and re-dip if the sealant is removed prior to calving. After calving, peel off any remaining teat dip prior to
milking. Consult your Ecolab representative for specific use instructions and recommended dispensing equipment. - KEEP OUT OF REACH OF CHILDREN
- SPL UNCLASSIFIED SECTION
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OTHER SAFETY INFORMATION
IF ON SKIN (or hair): Take off immediately all contaminated clothing. Rinse skin with water/shower. IF INHALED:
Remove person to fresh air and keep comfortable for breathing. Call a POISON CENTER/doctor if you feel unwell.
IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do.
Continue rinsing. If eye irritation persists: Get medical advice/attention. In case of fire: Use dry sand, dry
chemical or alcohol-resistant foam to extinguish.
READ SAFETY DATA SHEET (SDS) BEFORE USING THIS PRODUCT
EMERGENCY HEALTH INFORMATION: 1 800 328 0026. If located outside the United States and Canada,
call collect 1 651 222 5352 (number is in the US). - SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
UDDERGOLD DRY
polyvinylpyrrolidone solutionProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:47593-852 Route of Administration Topical Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POVIDONE, UNSPECIFIED (UNII: FZ989GH94E) (POVIDONE, UNSPECIFIED - UNII:FZ989GH94E) POVIDONE, UNSPECIFIED 0.910 g in 1 L Inactive Ingredients Ingredient Name Strength Alcohol (UNII: 3K9958V90M) ETHYL ACETATE (UNII: 76845O8NMZ) water (UNII: 059QF0KO0R) FLUORESCEIN (UNII: TPY09G7XIR) D&C RED NO. 28 (UNII: 767IP0Y5NH) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:47593-852-32 .95 L in 1 CONTAINER 2 NDC:47593-852-22 208 L in 1 CONTAINER Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 05/22/2022 Labeler - Ecolab Inc. (006154611)