Cardiotone

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Cardiotone
Generic name: ADENOSINUM TRIPHOSPHORICUM DINATRUM, CACTUS GRANDIFLORUS, CONVALLARIA MAJALIS, HEART (SUIS), MAGNESIUM GLUCONATE, POTASSIUM GLUCONATE, THYROIDINUM (SUIS), UBIDECARENONUM, GERMANIUM SESQUIOXIDE, STROPHANTHUS HISPIDUS, ADONIS VERNALIS, DIGITALIS PURPUREA
Manufacturer: BioActive Nutritional, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 282c9ee6-9be6-4ff0-9029-f778d6e9bf55
SPL ID: 26e8971c-369c-45e7-8b2a-c1c5c922b5f4
Version: 2
Effective date: 2024-08-28
Source export date: 2026-10-12
Source partition: 2
Source file: https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/4760f38f2bcb10aa20ddbadb42b270d31e9f2a8024440d3af3dec8d11feb92ec/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:28:14

Harmonized routes table
Harmonized routes
ORAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 20 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Cardiotone	openfda.brand_name
generic name		ADENOSINUM TRIPHOSPHORICUM DINATRUM, CACTUS GRANDIFLORUS, CONVALLARIA MAJALIS, HEART (SUIS), MAGNESIUM GLUCONATE, POTASSIUM GLUCONATE, THYROIDINUM (SUIS), UBIDECARENONUM, GERMANIUM SESQUIOXIDE, STROPHANTHUS HISPIDUS, ADONIS VERNALIS, DIGITALIS PURPUREA	openfda.generic_name
manufacturer name		BioActive Nutritional, Inc.	openfda.manufacturer_name
ndc	package	43857-0512-1	openfda.package_ndc
ndc	product	43857-0512	openfda.product_ndc
ndc11	package	43857051201	derived:openfda.package_ndc
spl id		26e8971c-369c-45e7-8b2a-c1c5c922b5f4	id
spl set id		282c9ee6-9be6-4ff0-9029-f778d6e9bf55	set_id
unii		6RV024OAUQ	openfda.unii
unii		EJ27X76M46	openfda.unii
unii		96WE91N25T	openfda.unii
unii		DX3ZNI25WK	openfda.unii
unii		T42NAD2KHC	openfda.unii
unii		12H3K5QKN9	openfda.unii
unii		5L51B4DR1G	openfda.unii
unii		X876KJM95L	openfda.unii
unii		QHH4HVF5QE	openfda.unii
unii		F1T8QT9U8B	openfda.unii
unii		MO892VI77K	openfda.unii
unii		7114SV0MYK	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS: 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.

Reported adverse events (FAERS/openFDA)#

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