ABS Valiant Catalyst (US)
- Manufacturer
- ABS Global Inc.
- Effective date
- 2019-07-09
- Label type
- OTC ANIMAL DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-01 02:40:28
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
SAFE HANDLING WARNING SECTION
KEEP OUT OF REACH OF CHILDREN
NOT FOR HUMAN USE
Danger
Causes severe skin burns and eye damage.
Wash skin thoroughly after handling. Wear protective gloves/ protective clothing/ eye protection/ face protection.
VETERINARY INDICATIONS SECTION
DIRECTIONS FOR USE
Use only in conjunction with Barrier (US), Pre (US) or Pre/Post (US) Teat Dip Products
Directions For Mixing: Add 3.5 ounces of Valiant Catalyst (US) to each gallon (27.3 mL Valiant Catalyst (US) to 1 liter) of Barrier (US), Pre (US) or Pre/Post (US) and mix using a mixing device recommended by your ABS representative. Proper mixing is very important, if you are mixing in drum quanities, a minimum of 3 complete turnovers of the contents is needed to properly activate Barrier (US), Pre (US) or Pre/Post (US) product. This mixed solution will remain stable for 7 days. After 7 days, discard solution and mix a new solution. In case of spill, rinse the area with large quantities of water.
IMPORTANT: Do not add Valiant Catalyst (US) to any teat dip other than Barrier (US), Pre (US) or Pre/Post (US) 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 Catalyst (US). See product labels for Barrier (US), Pre (US) or Pre/Post (US) products for complete directions for use.
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 or doctor/ physician. 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 or doctor/ physician. Wash contaminated clothing before reuse.
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).
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Valiant
quality milk system
Catalyst (US)
Unique Component for use only with Barrier (US), Pre (US) or Pre/Post (US) Base Products
An aid in reducing the spread of organisms which may cause mastitis.
ACTIVE INGREDIENT:
Stabilized Sodium Salt of Chlorous Acid ...................... 3.65%
INERT INGREDIENTS: ....... 96.35%
TOTAL: .................. 100.00%
3.78 L (1 US GAL)
Distributed by:
ABS Global, Inc. · P.O. Box 459 DeForest, Wisconsin USA 53532
Manufactured by:
Ecolab · 1 Ecolab Place ·
St. Paul MN 55102 USA ·
tel: 1 800 35 CLEAN (352 5326)
© 2016 Ecolab USA Inc ·
All rights reserved
Made in U.S.A.
www.ecolab.com · 767458/5300/1116
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 59282-105-11 | ABS Valiant Catalyst (US) | 3780 mL in 1 BOTTLE, PLASTIC | SOLUTION | 3780 | 1 | |
| 59282-105-42 | ABS Valiant Catalyst (US) | 5700 mL in 1 BOTTLE, PLASTIC | SOLUTION | 5700 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- ABS Valiant Catalyst (US)
- Stabilized Sodium Salt of Chlorous Acid
- SODIUM CHLORITE
- CHLORITE ION
- WATER
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 59282-105 | 59282-105-11, 59282-105-42 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| SODIUM CHLORITE | G538EBV4VF | ACTIB |
| WATER | 059QF0KO0R | IACT |
Source Document#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
