Label: ENCORE ACTIVATOR- chlorus acid solution
- NDC Code(s): 59282-108-17, 59282-108-21
- Packager: ABS Global 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 October 28, 2021
If you are a consumer or patient please visit this version.
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- SAFE HANDLING WARNING
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VETERINARY INDICATIONS
DIRECTIONS FOR USE
Mix Directions: Measure equal volumes of Encore Pre/Post & Encore Activator into clean containers. Mix until color is uniform. Mix a significant quantity for one milking and then discard the remainder.
IMPORTANT: Do not add mixed Encore Pre/Post & Encore Activator RTU (ready-to-use) to any other teat dip or other product. If transferred from this container to any other, make sure the other container is thoroughly pre-cleaned and bears the proper container labeling for Encore Pre/Post & Encore Activator RTU. Use of a complete udder health program including both pre- and post-dipping may aid reducing the spread of organisms which cause mastitis.
DIRECTIONS FOR TEAT DIPPING
Pre-Milking: Prepare teats prior to milking with appropriate pre-dip or udder wash. Teats should then be dried thoroughly with a single-service towel before attaching the milking unit.
Post-Milking: Immediately after milking, use Encore Pre/Post & Encore Activator RTU at full strength. Apply product to teats 2/3 their length in Encore Pre/Post & Encore Activator RTU teat dip. Allow to air dry. Do not wipe. Always use fresh, full-strength Encore
Pre/Post & Encore Activator RTU teat dip. If the product in the teat dip cup becomes visibly dirty, discard and replenish with fresh product. Do not reuse or return unused product to the original container. Do not turn cows into freezing weather until Encore Pre/Post & Encore Activator RTU teat dip is completely dry.
NOTE: In case of irritation or chapping, have the condition examined and, if necessary, treated by a veterinarian.
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OTHER SAFETY INFORMATION
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.
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).
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Principal display panel and representative label
ENCORE
Activator
Unique Component For Use Only With Encore Pre/Post
Activator – For use exclusively with Encore Pre/Post
An aid in reducing the spread of organisms which may cause mastitis.
ACTIVE INGREDIENTS:
Stabilized Sodium Salt of Chlorous Acid...............0.54%
INERT INGREDIENTS....................................99.46%
TOTAL:..........................................................100.00%
630065456.8 L (15 US GAL)
Distributed by:
ABS Global, Inc. ∙ P.O. Box 459
DeForest, Wisconsin USA 53532
www.absglobal.com
Manufactured by:
Ecolab Inc. ∙ 1 Ecolab Place ∙
St. Paul, MN 55102 USA ∙
tel. 1 800 392 3392
© 2018 Ecolab USA Inc ∙ All rights reserved
Made in U.S.A.
www.ecolab.com ∙ 753802/5301/1118
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INGREDIENTS AND APPEARANCE
ENCORE ACTIVATOR
chlorus acid solutionProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:59282-108 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHLOROUS ACID (UNII: 7JRT833T5M) (CHLOROUS ACID - UNII:7JRT833T5M) CHLOROUS ACID 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:59282-108-17 56780 mL in 1 DRUM 2 NDC:59282-108-21 208200 mL in 1 DRUM Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 03/30/2000 Labeler - ABS Global Inc. (835053570)