VALIANT PRE- lactic acid and linear dodecyl benzene sulfonic acid solution

Valiant Pre by

Drug Labeling and Warnings

Valiant Pre by is a Animal medication manufactured, distributed, or labeled by ABS Global Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SAFE HANDLING WARNING

KEEP OUT OF REACH OF CHILDREN

NOT FOR HUMAN USE

Warning

Causes eye irritation.

Wash skin thoroughly after handling.

Do not mix with bleach or other chlorinated products -

will cause chlorine gas.

For external use on dairy cows.

VETERINARY INDICATIONS

DIRECTIONS FOR USE

Mix Directions: Add 3.5 ounces of Valiant Catalyst (US)

to one gallon of Valiant Pre (US) or mix (27.3 mL Valiant

Catalyst (US) to 1 liter Valiant Pre (US)) and mix. Inverting

the container approximately 5-7 times will adequately

mix the two solutions. This mixed solution will remain

stable for 7 days. After 7 days, discard solution and mix a

new solution.

IMPORTANT: Do not add mixed Valiant Pre (US)

ready-to-use to any other teat dip or other products. If

transferred from this container to any other, make sure

the other container is thoroughly pre-cleaned and bears

the proper container labeling for Valiant Pre (US).

Use of a complete cow-care program including both

pre and post dipping may aid in reducing the spread of

organisms which may cause mastitis.

DIRECTIONS FOR PRE-MILKING

Fill teat dip cup with Valiant Pre (US). Before each cow

is milked, dip the teats as far as possible into the teat

dip cup containing Valiant Pre (US). Wipe teats dry after

dipping, using single-service towels to avoid

contamination of milk. Udder and teats which are

heavily soiled should be washed before using a

pre-milking teat dip. If product in dip cup becomes

visibly dirty, discard contents and replenish with fresh

product. Do not reuse or return unused product to the

original container.

NOTE: Valiant Pre (US) is not intended to cure or help in

the healing of chapped or irritated teats. In case of

irritation or chapping, have the condition examined

and, if necessary, treated by a veterinarian.

OTHER SAFETY INFORMATION

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.

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).

Representative label and principal display panel

Pre (US)

Valiant

Quality milk

System

Sanitizing Pre-Milking Teat Dip

Base – For use exclusively with Valiant Catalyst (US)

An aid in reducing the spread of organisms which may cause mastitis.

ACTIVE INGREDIENTS:

Lactic Acid............................................................................................................2.3%

Linear Dodecyl Benzene Sulfonic Acid ..................................................................1.6%

INERT INGREDIENTS:.........................................................................................96.1%

(contains lanolin and propylene glycol)

TOTAL:.............................................................................................................100.0%

6300465

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.

INGREDIENTS AND APPEARANCE

VALIANT PRE 
lactic acid and linear dodecyl benzene sulfonic acid solution

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 59282-101
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LACTIC ACID (UNII: 33X04XA5AT) (LACTIC ACID - UNII:33X04XA5AT)	LACTIC ACID	23 mg  in 1 mL
DODECYLBENZENESULFONIC ACID (UNII: 60NSK897G9) (DODECYLBENZENESULFONIC ACID - UNII:60NSK897G9)	DODECYLBENZENESULFONIC ACID	16 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59282-101-16	18930 mL in 1 PAIL
2	NDC: 59282-101-17	56780 mL in 1 DRUM
3	NDC: 59282-101-21	208200 mL in 1 DRUM
4	NDC: 59282-101-44	1135000 mL in 1 CONTAINER

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)