FDA.reportPublic FDA data

Arrhythmiaforce

Manufacturer
BioActive Nutritional, Inc. | Apotheca Company
Effective date
2021-06-21
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:43:07

Label at a glance#

ProductArrhythmiaforce
Active ingredientBLACK WALNUT, LEONURUS CARDIACA, ADONIS VERNALIS, CONVALLARIA MAJALIS, MAGNESIUM SULFATE HEPTAHYDRATE, POTASSIUM CHLORATE, IBERIS AMARA SEED, DIGITALIS, LYCOPUS VIRGINICUS, PHOSPHORUS
Label structure9 sections

Dosage and administration

10 drops orally, 3 times a day. Consult a physician for use in children under 12 years of age.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Juglans Nigra 3X, Leonurus Cardiaca 3X, Adonis Vernalis 4X, Convallaria Majalis 4X, Magnesia Sulphurica 4X, Kali Chloricum 6X, Iberis Amara 6X, Digitalis Purpurea 12X, Lycopus Virginicus 12X, Phosphorus 12X.

INDICATIONS:

OTC - PURPOSE SECTION

For temporary relief of lightheadedness & nervous anxiety, dizziness on rising or lying down, sensation as if heart stops and then starts again.

WARNINGS:

WARNINGS SECTION

If pregnant or breast-feeding, ask a health care professional before use.

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Do not use if tamper evident seal is broken or missing.

Store in cool, dry place.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

10 drops orally, 3 times a day. Consult a physician for use in children under 12 years of age.

INDICATIONS:

INDICATIONS & USAGE SECTION

For temporary relief of lightheadedness & nervous anxiety, dizziness on rising or lying down, sensation as if heart stops and then starts again.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized Water, 25% Ethanol.

QUESTIONS:

OTC - QUESTIONS SECTION

Distributed by:

BioActive Nutritional, Inc.

1803 N. Wickham Rd.

Melbourne, FL 32935

bioactivenutritional.com

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BIOActive Nutritional

ARRHYTHMIAFORCE

HOMEOPATHIC

1 FL OZ (30 ml)

ArrhythmiaforceArrhythmiaforce

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43857-043343857-0433-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
BLACK WALNUT02WM57RXZJACTIB
LEONURUS CARDIACA8NC0C2YXK0ACTIB
ADONIS VERNALISDX3ZNI25WKACTIB
CONVALLARIA MAJALISQHH4HVF5QEACTIB
MAGNESIUM SULFATE HEPTAHYDRATESK47B8698TACTIB
POTASSIUM CHLORATEH35KS68EE7ACTIB
IBERIS AMARA SEEDT90A7M66YFACTIB
DIGITALISF1T8QT9U8BACTIB
LYCOPUS VIRGINICUSTWH5125Q6FACTIB
PHOSPHORUS27YLU75U4WACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT

Source Document#

Source XML · Source PDF

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
c1d4830d-3b43-43d8-af89-a5a6f3dcc0f39591e95b-e099-496c-96c6-3c2f0f0e330b2021-06-21WarningsExact identifier
spl id: c1d4830d-3b43-43d8-af89-a5a6f3dcc0f3
spl set id: 9591e95b-e099-496c-96c6-3c2f0f0e330b

Reported adverse events (FAERS/openFDA)#

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