FDA.reportPublic FDA data

Cardioforce

Manufacturer
BioActive Nutritional, Inc. | Apotheca Company
Effective date
2024-10-17
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:28:14

Label at a glance#

ProductCardioforce I
Active ingredientARNICA MONTANA WHOLE, SELENICEREUS GRANDIFLORUS STEM, CAPSICUM, DIGITALIS, POTASSIUM PHOSPHATE, DIBASIC, PRUNUS LAUROCERASUS LEAF, SPIGELIA ANTHELMIA WHOLE, TOBACCO LEAF, ACONITUM NAPELLUS WHOLE, AMANITA MUSCARIA FRUITING BODY, GOLD TRICHLORIDE, NITROGLYCERIN, STRYCHNOS IGNATII SEED, KALMIA LATIFOLIA LEAF, LATRODECTUS MACTANS, VALERIAN
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

Arnica Montana 3X, Cactus Grandiflorus 3X, Capsicum Annuum 3X, Digitalis Purpurea 6X, Kali Phosphoricum 6X, Laurocerasus 6X, Spigelia Anthelmia 3X, Tabacum 6X, Aconitum Napellus 12X, Aurum Muriaticum 12X, Glonoinum 12X, Ignatia Amara 12X, Kalmia Latifolia 12X, Latrodectus Mactans 12X, Valeriana Officinalis 12X.

INDICATIONS:

OTC - PURPOSE SECTION

For temporary relief of heaviness of the chest, tiredness after minimal exercise, difficulty breathing with heaviness.

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 a 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 heaviness of the chest, tiredness after minimal exercise, difficulty breathing with heaviness.

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

CARDIOFORCE I

HOMEOPATHIC

1 FL OZ (30 ml)

Cardioforce ICardioforce I

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7480e90b-004b-ebe4-2243-4f2fefdd9e78Product name220260128
3f158398-73f2-4b90-47d1-5c60e8719a98Product name920250721
efd58dcf-540a-4531-8766-e713129ca6f2Product name120250307
4b7700e3-6e0e-45e5-9d22-6f754d61386eProduct name220250304
726062af-1135-4707-a1d7-57256991bbf9Product name220250226
ca6149a6-ded3-9f17-6c41-3e88f2c0c9c0Product name220250117
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
00358076-c817-430b-b924-11d717dc307cProduct name120160718
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
19c71a3d-ed9c-166b-a7e5-38c250c35631Product name120140508
669af5aa-14f3-3df7-f100-5f580ffd43c1Product name120140508
6ff3bab7-2dce-8bea-d7ce-54687f0c01fbProduct name120140508
8bb82a1c-d0d0-fc27-011f-172e545f0382Product name120140508
cb03406d-e223-80bb-67d8-be80f9b6a4f2Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43857-0442-1CardioforceI30 mL in 1 BOTTLE, DROPPERLIQUID302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43857-0442CARDIOFORCE I (ARNICA MONTANA, CACTUS GRANDIFLORUS, CAPSICUM ANNUUM, DIGITALIS PURPUREA, KALI PHOSPHORICUM, LAUROCERASUS, SPIGELIA ANTHELMIA, TABACUM, ACONITUM NAPELLUS, AGARICUS MUSCARIUS, AURUM MURIATICUM, GLONOINUM, IGNATIA AMARA, KALMIA LATIFOLIA, LATRODECTUS MACTANS, VALERIANA OFFICINALIS) LIQUID [BIOACTIVE NUTRITIONAL, INC.]2Current NDC, Legacy NDC, 1 package rows20241019_0bb404b6-a7c1-4077-995e-d7ce59409a29.zip

Products#

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

DailyMed product names page 1 of 1 · 25 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43857-044243857-0442-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
ARNICA MONTANA WHOLEO80TY208ZWACTIB
SELENICEREUS GRANDIFLORUS STEM7114SV0MYKACTIB
CAPSICUM00UK7646FGACTIB
DIGITALISF1T8QT9U8BACTIB
POTASSIUM PHOSPHATE, DIBASICCI71S98N1ZACTIB
PRUNUS LAUROCERASUS LEAFF26P2D4757ACTIB
SPIGELIA ANTHELMIA WHOLEWYT05213GEACTIB
TOBACCO LEAF6YR2608RSUACTIB
ACONITUM NAPELLUS WHOLEU0NQ8555JDACTIB
AMANITA MUSCARIA FRUITING BODYDIF093I037ACTIB
GOLD TRICHLORIDE15443PR153ACTIB
NITROGLYCERING59M7S0WS3ACTIB
STRYCHNOS IGNATII SEED1NM3M2487KACTIB
KALMIA LATIFOLIA LEAF79N6542N18ACTIB
LATRODECTUS MACTANSXJJ7QA858RACTIB
VALERIANJWF5YAW3QWACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT

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
Cardioforce IARNICA MONTANA, CACTUS GRANDIFLORUS, CAPSICUM ANNUUM, DIGITALIS PURPUREA, KALI PHOSPHORICUM, LAUROCERASUS, SPIGELIA ANTHELMIA, TABACUM, ACONITUM NAPELLUS, AGARICUS MUSCARIUS, AURUM MURIATICUM, GLONOINUM, IGNATIA AMARA, KALMIA LATIFOLIA, LATRODECTUS MACTANS, VALERIANA OFFICINALISBioActive Nutritional, Inc.0bb404b6-a7c1-4077-995e-d7ce59409a292024-10-17WarningsExact identifier
ndc (package): 43857-0442-1
ndc (product): 43857-0442
ndc11 (package): 43857044201
spl id: 2d52d5ef-5023-40d2-9ff4-0fd277db68ec
spl set id: 0bb404b6-a7c1-4077-995e-d7ce59409a29

Reported adverse events (FAERS/openFDA)#

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