PRITOX

Manufacturer
FIRST PRIORITY INCORPORATED
Effective date
2023-12-04
Label type
OTC ANIMAL DRUG LABEL
Version
11
Source
full-release
Hydrated at
2026-06-01 02:42:35

Label at a glance#

ProductPRITOX
Active ingredientCOPPER NAPHTHENATE
Label structure11 sections

Dosage and administration

Clean the hoof thoroughly, removing debris and necrotic material prior to application of Pritox ® . Apply daily to affected hoofs with a narrow paint brush (about 1") until fully healed. Caution: Do not allow runoff of excess Pritox ® onto hair since contact with Pritox ® may cause some hair loss.  Do not contaminate feed.

Storage and handling

Store at controlled room temperature 15° to 30°C (59° to 86°F). Keep container tightly closed when not in use. Manufactured By: FIRST PRIORITY, INC., Elgin, IL 60123 Made in U.S.A www.prioritycare.com NOT RETURNABLE IF OUTDATED Reorder No. TP281PC (16 oz) Lot No. Exp. Date Priority Care and Pritox are registered trademarks of First Priority, Inc. Rev. 10-22

Label contents#

Full prescribing information#

INFORMATION FOR OWNERS/CAREGIVERS SECTION

(copper naphthenate)

Water-Resistant Protection Without Bandaging

Recommended as an Aid in Treating Horses and Ponies With Thrush Due to Organisms Susceptible to Copper Naphthenate.

Do Not Use in Horses Intended for Human Consumption.

FOR EXTERNAL USE ONLY

CAUTION: COMBUSTIBLE MIXTURE

Not for Use in Humans • Keep Out of Reach of Children

INDICATIONS:

INDICATIONS & USAGE SECTION

Pritox® is indicated in the treatment of thrush in horses and ponies.

GENERAL DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Clean the hoof thoroughly, removing debris and necrotic material prior to application of Pritox®. Apply daily to affected hoofs with a narrow paint brush (about 1") until fully healed. Caution: Do not allow runoff of excess Pritox® onto hair since contact with Pritox® may cause some hair loss.  Do not contaminate feed.

INFORMATION FOR OWNERS/CAREGIVERS SECTION

NOTE: Pritox® is easily removed from hands, clothing and surfaces with light grade fuel oil or any type of lighter fluid.

CONTAINS FOIL SEAL – REMOVE BEFORE USE.

SHAKE WELL BEFORE USE.

ADVERSE REACTIONS SECTION

To report suspected adverse events, for technical assistance or to obtain a copy of the Safety Data Sheet (SDS), contact First Priority, Inc. at (800) 650-4899 or www.prioritycare.com.
For additional information about adverse drug experience reporting for animal drugs, contact FDA at 1-888-FDA-VETS or www.fda.gov/reportanimalae

image of eye clockimage of eye clock

ACTIVE INGREDIENT:

OTC - ACTIVE INGREDIENT SECTION

Copper Naphthenate .....37.5% w/w

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

... 62.5% w/w
Total.................................... 100.0%

CAUTION:

PRECAUTIONS SECTION

Do not use in horses intended for human consumption.

CAUTION: COMBUSTIBLE MIXTURE.

Use in a well-ventilated place. Avoid fire, flame, sparks or heaters.

If swallowed, do not induce vomiting, call physician immediately. Avoid breathing vapor. Avoid contact with skin and eyes.

KEEP OUT OF REACH OF CHILDREN AND PETS.

STORAGE:

STORAGE AND HANDLING SECTION

Store at controlled room temperature 15° to 30°C (59° to 86°F). Keep container tightly closed when not in use.

Manufactured By:
FIRST PRIORITY, INC., Elgin, IL 60123

Made in U.S.A

www.prioritycare.com

NOT RETURNABLE IF OUTDATED

Reorder No. TP281PC (16 oz)

Lot No. Exp. Date

Priority Care and Pritox are registered trademarks of First Priority, Inc.

Rev. 10-22

Net Contents:

HOW SUPPLIED SECTION

16 oz (473 mL)

16 oz (473 mL)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of 473 mL bottle/case labelimage of 473 mL bottle/case label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1373395copper naphthenate 37.5 % Topical SolutionPSN11
1373400Pritox 37.5 % Water Resistant Topical SolutionPSN11
1373400copper naphthenate 375 MG/ML Topical Solution [Pritox]SBD11
1373395copper naphthenate 375 MG/ML Topical SolutionSCD11
1373395copper naphthenate 37.5 % Topical SolutionSY11
1373400Pritox 37.5 % Topical SolutionSY11
1373400Pritox 375 MG/ML Topical SolutionSY11

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
COPPER Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c599c4a0-705d-4ebb-ab1f-977af038f96aProduct name120251124

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58829-289-16PRITOX473 mL in 1 BOTTLE, DISPENSINGLIQUID47311
58829-289-16PRITOX12 in 1 CASELIQUID1211

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58829-289PRITOX (COPPER NAPHTHENATE) LIQUID [FIRST PRIORITY INCORPORATED]112 package rows20231205_dd0e7c46-9e9b-43f7-b5a1-42977c006eaf.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
COPPER NAPHTHENATEACTIVE INGREDIENT9J2IBN2H706
COPPERACTIVE MOIETY789U1901C56

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
58829-28958829-289-16

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
COPPER NAPHTHENATE9J2IBN2H70ACTIB

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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