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#

ProductABS Valiant Catalyst (US)
Active ingredientSODIUM CHLORITE
Label structure4 sections

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

www.absglobal.com

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

Representative labelRepresentative label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59282-105-11ABS Valiant Catalyst (US)3780 mL in 1 BOTTLE, PLASTICSOLUTION37801
59282-105-42ABS Valiant Catalyst (US)5700 mL in 1 BOTTLE, PLASTICSOLUTION57001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59282-105ABS VALIANT CATALYST (US) (STABILIZED SODIUM SALT OF CHLOROUS ACID) SOLUTION [ABS GLOBAL INC.]12 package rows20190710_af10e9a7-0e5b-47a6-93af-b153f8a7db7b.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59282-10559282-105-11, 59282-105-42

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
SODIUM CHLORITEG538EBV4VFACTIB
WATER059QF0KO0RIACT

Source Document#

Source XML

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.

Matched openFDA labels page 1 of 1 · 11 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Doctor GuardStickSODIUM CHLORITEPure O2a39b49fd-9eac-73b4-e053-2995a90a180d2023-11-16WarningsName fallback
generic name: SODIUM CHLORITE
PURE O2STICKSODIUM CHLORITEPure O2a39a1e99-d714-645d-e053-2995a90a024c2023-11-16WarningsName fallback
generic name: SODIUM CHLORITE
EasyStickSODIUM CHLORITEPure O2a39b9ce6-a074-4165-e053-2995a90a277a2023-11-16WarningsName fallback
generic name: SODIUM CHLORITE
iSTICKSODIUM CHLORITEPure O2a6f7ea11-3cbe-6739-e053-2a95a90a41cf2023-11-16WarningsName fallback
generic name: SODIUM CHLORITE
NARYN CARE StickSODIUM CHLORITEPure O2a6fb2adf-5312-84c4-e053-2a95a90a5ded2023-11-16WarningsName fallback
generic name: SODIUM CHLORITE
D.PRO Pack SolidSODIUM CHLORITEPure O2c0289ea3-c592-0760-e053-2a95a90a0cfd2021-04-17WarningsName fallback
generic name: SODIUM CHLORITE
DEFENDERSTICKSODIUM CHLORITEPure O2c02915ef-e7fc-4811-e053-2a95a90a97702021-04-17WarningsName fallback
generic name: SODIUM CHLORITE
DEFENDER SIGNATURESODIUM CHLORITEPure O2c029345a-d44b-74db-e053-2995a90a1dbe2021-04-17WarningsName fallback
generic name: SODIUM CHLORITE
PURE O2 Pack-SolidSODIUM CHLORITEPure O2a397afb9-53a7-e6d8-e053-2a95a90a54d42020-08-29WarningsName fallback
generic name: SODIUM CHLORITE
QVE - SSODIUM CHLORITEPure O2acdeca69-4e20-9502-e053-2a95a90a53272020-08-14WarningsName fallback
generic name: SODIUM CHLORITE
V Doctor pure chlorine dioxideSODIUM CHLORITEPure O2a492a03c-c28e-fcd6-e053-2a95a90a65d42020-05-01WarningsName fallback
generic name: SODIUM CHLORITE

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.