Label: ENCORE PRE/POST- lactic acid solution
- NDC Code(s): 59282-107-17, 59282-107-21
- 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 June 24, 2019
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
-
SAFE HANDLING WARNING
KEEP OUT OF REACH OF CHILDREN
NOT FOR HUMAN USE
Attention
For External Use Only
Wash hands thoroughly after handling. Do not mix
with bleach or other chlorinated products – will cause
chlorine gas.
Get medical advice/ attention if you feel unwell.
Read Safety Data Sheet (SDS) before using this
product.
-
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.
- OTHER SAFETY INFORMATION
-
Representative label and principal display panel
Pre/Post
Sanitizing Pre/Post Teat Dip
Base – For use exclusively with Encore Activator
An aid in reducing the spread of organisms which may cause mastitis.
ACTIVE INGREDIENT:
Lactic acid.........................................................................................................................2.64%
INERT INGREDIENTS:................................................................................................ 97.36%
(contains sorbitol, PEG-75 lanolin)
TOTAL:..........................................................................................................................100.00%
6300651
208 L (55 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 ∙ 753796/5302/1118
-
INGREDIENTS AND APPEARANCE
ENCORE PRE/POST
lactic acid solutionProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:59282-107 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LACTIC ACID (UNII: 33X04XA5AT) (LACTIC ACID - UNII:33X04XA5AT) LACTIC ACID 26.4 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SORBITOL (UNII: 506T60A25R) PEG-75 LANOLIN (UNII: 09179OX7TB) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59282-107-17 56780 mL in 1 DRUM 2 NDC:59282-107-21 208200 mL in 1 DRUM Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/16/2005 Labeler - ABS Global Inc. (835053570)