Arteriotone

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: Arteriotone
Generic name: BAPTISIA TINCTORIA, CACTUS GRANDIFLORUS, ECHINACEA (ANGUSTIFOLIA), ADONIS VERNALIS, AGNUS CASTUS, ARNICA MONTANA, AURUM METALLICUM, DIGITALIS PURPUREA, GLONOINUM, VANADIUM METALLICUM
Manufacturer: Energique, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 4bb46cf1-bfcb-4d57-a982-7ba87e2b299a
SPL ID: 33a86817-1d07-4e87-90c2-11d12edae391
Version: 6
Effective date: 2024-07-16
Source export date: 2026-09-28
Source partition: 6
Source file: https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:37:07

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 · 18 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Arteriotone	openfda.brand_name
generic name		BAPTISIA TINCTORIA, CACTUS GRANDIFLORUS, ECHINACEA (ANGUSTIFOLIA), ADONIS VERNALIS, AGNUS CASTUS, ARNICA MONTANA, AURUM METALLICUM, DIGITALIS PURPUREA, GLONOINUM, VANADIUM METALLICUM	openfda.generic_name
manufacturer name		Energique, Inc.	openfda.manufacturer_name
ndc	package	44911-0230-1	openfda.package_ndc
ndc	product	44911-0230	openfda.product_ndc
ndc11	package	44911023001	derived:openfda.package_ndc
spl id		33a86817-1d07-4e87-90c2-11d12edae391	id
spl set id		4bb46cf1-bfcb-4d57-a982-7ba87e2b299a	set_id
unii		DX3ZNI25WK	openfda.unii
unii		O80TY208ZW	openfda.unii
unii		79Y1949PYO	openfda.unii
unii		VB06AV5US8	openfda.unii
unii		433OSF3U8A	openfda.unii
unii		00J9J9XKDE	openfda.unii
unii		G59M7S0WS3	openfda.unii
unii		5EF0HWI5WU	openfda.unii
unii		F1T8QT9U8B	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 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.