Euthanasia Solution

Manufacturer
MWI Veterinary Supply
Effective date
2025-12-19
Label type
PRESCRIPTION ANIMAL DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:45:37

Label at a glance#

ProductEuthanasia Solution
Active ingredientpentobarbital sodium, phenytoin sodium
Label structure11 sections

Dosage and administration

Dosage: Dogs, 1 mL for each 10 pounds of body weight. Administration: Intravenous injection is preferred. Intracardiac injection may be made when intravenous injection is impractical, as in a very small dog, or in a comatose dog with impaired vascular functions. Good injection skill is necessary for intracardiac injection. The calculated dose should be given in a single bolus injection. For intravenous injection, ...

Label contents#

Full prescribing information#

CAUTION:

GENERAL PRECAUTIONS SECTION

Federal law restricts this drug to use by or on the order of a licensed veterinarian.

DESCRIPTION:

DESCRIPTION SECTION

A non-sterile solution containing pentobarbital sodium and phenytoin sodium as the active ingredients. Rhodamine B, a bluish-red fluorescent dye, is included in the formulation to help distinguish it from parenteral drugs intended for therapeutic use. Although the solution is not sterile, benzyl alcohol, a bacteriostat, is included to retard the growth of microorganisms.

Each mL contains:Active ingredients: 390 mg pentobarbital sodium (barbituric acid derivative), 50 mg phenytoin sodium; Inactive ingredients: 10% ethyl alcohol, 18% propylene glycol, 0.003688 mg rhodamine B, 2% benzyl alcohol (preservative), water for injection q.s. Sodium hydroxide and/or hydrochloric acid may be added to adjust pH.

ACTIONS:

SPL UNCLASSIFIED SECTION

Euthanasia Solution contains two active ingredients which are chemically compatible but pharmacologically different. Each ingredient acts in such a manner so as to cause humane, painless, and rapid euthanasia. Euthanasia is due to cerebral death in conjunction with respiratory arrest and circulatory collapse. Cerebral death occurs prior to cessation of cardiac activity.

When administered intravenously, pentobarbital sodium produces rapid anesthetic action. There is a smooth and rapid onset of unconsciousness. At the lethal dose, there is depression of vital medullary respiratory and vasomotor centers.

When administered intravenously, phenytoin sodium produces toxic signs of cardiovascular collapse and/or central nervous system depression. Hypotension occurs when the drug is administered rapidly.

Pharmacodynamic Activity: The sequence of events leading to humane, painless, and rapid euthanasia following intravenous injection of Euthanasia Solution is similar to that following intravenous injection of pentobarbital sodium or other barbituric acid derivatives. Within seconds, unconsciousness is induced with simultaneous collapse of the dog. This stage rapidly progresses to deep anesthesia with concomitant reduction in
the blood pressure. A few seconds later, breathing stops, due to depression of the medullary respiratory center; encephalographic activity becomes isoelectric, indicating cerebral death, and then cardiac activity ceases. Phenytoin sodium exerts its effect during the deep anesthesia stage caused by the pentobarbital sodium. This ingredient, due to its cardiotoxic properties, hastens the stoppage of electrical activity in the heart.

INDICATIONS:

INDICATIONS & USAGE SECTION

For use in dogs for humane, painless, and rapid euthanasia.

WARNING:

WARNINGS SECTION

For canine euthanasia only. Must not be used for therapeutic purposes. Do not use in animals intended for food.

ENVIRONMENTAL WARNING SECTION

ENVIRONMENTAL HAZARD: This product is toxic to wildlife. Birds and mammals feeding on treated animals may be killed. Euthanized animals must be properly disposed of by deep burial, incineration, or other method in compliance with state and local laws, to prevent consumption of carcass material by scavenging wildlife.

HUMAN WARNING:

USER SAFETY WARNINGS SECTION

Caution should be exercised to avoid contact of the drug with open wounds or accidental self-inflicted injections. Keep out of reach of children. If eye contact, flush with water and seek medical advice/attention.

PRECAUTIONS:

PRECAUTIONS SECTION

Euthanasia may sometimes be delayed in dogs with severe cardiac or circulatory deficiencies. This may be explained by the impaired movement of the drug to its site of action. An occasional dog may elicit reflex responses manifested by motor movement; however, an unconscious animal does not experience pain, because the cerebral cortex is not functioning.

When restraint may cause the dog pain, injury, or anxiety, or danger to the person making the injection, prior use of tranquilizing or immobilizing drugs may be necessary.

Dosage and Administration:

DOSAGE & ADMINISTRATION SECTION

Dosage: Dogs, 1 mL for each 10 pounds of body weight.

Administration: Intravenous injection is preferred. Intracardiac injection may be made when intravenous injection is impractical, as in a very small dog, or in a comatose dog with impaired vascular functions. Good injection skill is necessary for intracardiac injection.

The calculated dose should be given in a single bolus injection.

For intravenous injection, a needle of sufficient gauge to ensure intravenous placement of the entire dose should be used. The use of a Luer-Lok® syringe is recommended to prevent accidental exposure due to needle/syringe separation.

ADVERSE REACTION:

ADVERSE REACTIONS SECTION

To report suspected adverse events, for technical assistance or to obtain a copy of the Safety Data Sheet (SDS), contact the technical help-line at
866-489-1344. For additional information about adverse drug experience reporting for animal drugs,contact FDA at 1-888-FDA-VETS or online at www.fda.gov/reportanimalae.

HOW SUPPLIED:

HOW SUPPLIED SECTION

Euthanasia Solution (Pentobarbital Sodium and Phenytoin Sodium) is available in 100 ml multi-dose vials in package of one, NDC 86136-138-31.

Manufactured by a nonsterilizing process.

STORAGE:

STORAGE AND HANDLING SECTION

Store at controlled room temperature 20° to 25°C (68° to 77°F). Use contents within 60 days of first puncture. Approved by FDA under ANADA #200-614

SPL UNCLASSIFIED SECTION

Distributed by: MWI
Boise, ID, 83705
www.VetOne.net

lss. 10/2025

Luer-Lok is a registered trademark of Becton, Dickinson and Company.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of 100mL vial labelImage of 100mL vial label

SPL UNCLASSIFIED SECTION

Image of 100mL cartonImage of 100mL carton

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1100449PENTobarbital sodium 390 MG/mL / phenytoin sodium 50 MG/mL Injectable SolutionPSN3
1100449pentobarbital sodium 390 MG/ML / phenytoin sodium 50 MG/ML Injectable SolutionSCD3
1100449Pentobarbital Sodium 390 MG/ML / DPH sodium 50 MG/ML Injectable SolutionSY3

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
PHENYTOIN Pharmacologic Class Indexing4Indexing - Pharmacologic Class20181113

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130386136138313GTIN-13: 0386136138313
EAN-13: 0386136138313
GTIN-12: 386136138313
UPC-A: 386136138313
GTIN storage (14 digits): 00386136138313
VetOne_Label.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
be8c0c29-be12-4cae-8e3b-1c71ed6b952cProduct name220250626
e3d31abf-5149-4e77-89a8-0dc73ec106f9Product name120210525
b251e19b-cfda-4a5c-8c9c-f4dad5d55ecbProduct name220200303
a608f88c-baa8-0098-ce26-66cf9faa6b64Product name320180110
031bbc61-0564-1f35-2716-aa5c1d139248Product name220141218
cc830ceb-037c-a5c3-ee14-3d82c0e89e70Product name120140508
eafc3fd3-6834-3129-5bbb-8a9a495691abProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
86136-138-31Euthanasia Solution100 mL in 1 VIAL, MULTI-DOSESOLUTION1003

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
86136-13886136-138-31

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
pentobarbital sodiumNJJ0475N0SACTIB
phenytoin sodium4182431BJHACTIB

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 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Pentobarbital SodiumPENTOBARBITAL SODIUMHikma Pharmaceuticals USA Inc.d375b92a-baa1-4d63-9ad1-1467dcfde7d52024-03-08Warnings, Adverse reactionsName fallback
generic name: PENTOBARBITAL SODIUM

Reported adverse events (FAERS/openFDA)#

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