Label: 4XLA BASE- sodium chlorite solution
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NDC Code(s):
47593-607-04,
47593-607-16,
47593-607-17,
47593-607-21, view more47593-607-44
- 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 13, 2023
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
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SAFE HANDLING WARNING
FOR USE ONLY WITH 4XLA® ACTIVATOR
DANGER: Causes severe skin burns and eye damage. Wash skin thoroughly after handling. Wear protective gloves/ protective clothing/ eye protection/ face protection.
DISPOSAL: Unused teat dip may be diluted with water and flushed down drain. Do not reuse containers. Empty containers should be thoroughly rinsed with water and taken to a recycling center.
KEEP OUT OF THE REACH OF CHILDREN
NOT FOR HUMAN USE
AVOID FREEZING: If product is exposed to freezing temperatures, components must be mixed thoroughly prior to use.
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VETERINARY INDICATIONS
DIRECTIONS FOR USE: Measure equal volumes of 4XLA® base and 4XLA activator into a clean dip cup/container and mix until the color is uniform through-out. Do not dilute. Mix only enough product for one milking of the herd. Dip cups should be washed after each milking.
APPLICATION:
Pre-Milking: If teats are visibly dirty, wash and dry teats with a single service towel prior to dipping. Before each cow is milked, dip the teats as far up as possible. Leave 4XLA Teat Dip on teats for at least 15-30 seconds. Wipe teats dry using a single service towel before milking.
Post-Milking: Immediately after milking, dip teats at least 2/3 to all their length in 4XLA Teat Dip. Allow to air dry. DO NOT WIPE. 4XLA Teat Dip can be used as a post-dip alone, or as a pre- and post-milking teat dip.
Always use freshly mixed, full strength 4XLA Teat Dip. If product in dip cup becomes visibly dirty, discard contents and fill with fresh 4XLA Teat Dip.
Note 1: If teat irritation occurs, discontinue use until irritation subsides. Consult your veterinarian and milking equipment service personnel if irritation persists.
Note 2: The gold color in the mixed product fades with time. At higher temperatures the fading is more rapid. However, this will not affect the efficacy of the product.
Note 3: 4XLA should be used only with a compatible pre-dip or udder wash.
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OTHER SAFETY INFORMATION
IF SWALLOWED: Rinse mouth. Do NOT induce vomiting. 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. Immediately call a POISON CENTER/ doctor. IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. Immediately call a POISON CENTER/ doctor. Wash contaminated clothing before reuse.
READ SAFETY DATA SHEET (SDS) BEFORE USING THIS PRODUCT
FOR EMERGENCY MEDICAL INFORMATION IN USA OR CANADA, CALL: 1-800-328-0026.
FOR EMERGENCY MEDICAL INFORMATION WORLDWIDE, CALL: 1-651-222-5352 (IN THE USA).
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Principal display panel and representative container
4XLA 6302478
GERMICIDAL PRE- & POST-MILKING TEAT DIP
An aid in reducing the spread of organisms which may cause mastitis
BASE
ACTIVE INGREDIENT:
Sodium Chlorite................................................... 0.6%
INERT INGREDIENTS:....................................... 99.4%
TOTAL:.............................................................. 100.0%
208 L (55 US GAL)
Manufactured by | Fabricado por Ecolab · 1 Ecolab Place · St. Paul, MN 55102 USA · tel: 1 800 392 3392
© 2021 Ecolab USA · All rights reserved | Todos los derechos reservados
Made in U.S.A. | Hecho en EE. UU. www.ecolab.com · 766662/5301/1121
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INGREDIENTS AND APPEARANCE
4XLA BASE
sodium chlorite solutionProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:47593-607 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM CHLORITE (UNII: G538EBV4VF) (CHLORITE ION - UNII:Z63H374SB6) SODIUM CHLORITE 6 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:47593-607-16 18900 mL in 1 PAIL 2 NDC:47593-607-17 56800 mL in 1 DRUM 3 NDC:47593-607-04 54800 mL in 1 DRUM 4 NDC:47593-607-21 208000 mL in 1 DRUM 5 NDC:47593-607-44 1134000 mL in 1 CONTAINER Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 05/08/2014 Labeler - Ecolab Inc. (006154611)