FDA.reportPublic FDA data

HEARTBEATPET

Manufacturer
Groupe Cyrenne Inc. | Laboratoire Schmidt-Nagel Inc
Effective date
2025-12-17
Label type
OTC ANIMAL DRUG LABEL
Version
6
Source
monthly-update
Hydrated at
2026-06-03 17:44:59

Label at a glance#

ProductHEARTBEATPET
Active ingredientBOTHROPS ATROX VENOM, SELENICEREUS GRANDIFLORUS STEM, LYCOPUS VIRGINICUS WHOLE, NAJA KAOUTHIA WHOLE, NITROGLYCERIN, DIGITALIS
Label structure7 sections

Indications and uses

Helps maintain a regular and steady heartbeat. For cats and dogs only.

Label contents#

Full prescribing information#

Active ingredients                                     Purpose

OTC - ACTIVE INGREDIENT SECTION

Bothrops Lanceolatus 30k                         Chest pain

Cactus Grandiflorus 30k                            Constriction of the heart

Lycopus Virginicus 30k                              Irregular heartbeat

Naja Tripudians 30k                                  Palpitations of the heart

Glonoinum 30k                                        Rapid pulse

Digitalis Purpurea 30k                              Slow heartbeat

Uses

INDICATIONS & USAGE SECTION

Helps maintain a regular and steady heartbeat. For cats and dogs only.

Warning

WARNINGS SECTION

Keep out of reach of children.

Direction

DOSAGE & ADMINISTRATION SECTION

1 spray every day, in water or directly in the mouth. Stop when symptoms disappear. Not for prevention.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Ethyl alcohol 20%, purified water

Cautions

SPL UNCLASSIFIED SECTION

Shake well before use. Respect the dosage. Essential oils can negate the effects of homeopathic products. Store in a cool place away from direct sunlight.

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7480e90b-004b-ebe4-2243-4f2fefdd9e78Product name220260128
3f158398-73f2-4b90-47d1-5c60e8719a98Product name920250721
ca6149a6-ded3-9f17-6c41-3e88f2c0c9c0Product name220250117
00358076-c817-430b-b924-11d717dc307cProduct name120160718
669af5aa-14f3-3df7-f100-5f580ffd43c1Product name120140508
6ff3bab7-2dce-8bea-d7ce-54687f0c01fbProduct name120140508
8bb82a1c-d0d0-fc27-011f-172e545f0382Product name120140508
cb03406d-e223-80bb-67d8-be80f9b6a4f2Product name120140508

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
86147-05186147-051-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
BOTHROPS ATROX VENOMK0Q6REZ9JCACTIB
SELENICEREUS GRANDIFLORUS STEM7114SV0MYKACTIB
LYCOPUS VIRGINICUS WHOLETWH5125Q6FACTIB
NAJA KAOUTHIA WHOLEB1AGI4NK4ZACTIB
NITROGLYCERING59M7S0WS3ACTIB
DIGITALISF1T8QT9U8BACTIB
ALCOHOL3K9958V90MIACT
WATER059QF0KO0RIACT

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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