FDA.reportPublic FDA data

Arteriotone

Manufacturer
Energique, Inc. | Apotheca Company
Effective date
2024-07-16
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 02:27:33

Label at a glance#

ProductArteriotone
Active ingredientBAPTISIA TINCTORIA ROOT, SELENICEREUS GRANDIFLORUS STEM, ECHINACEA ANGUSTIFOLIA WHOLE, ADONIS VERNALIS WHOLE, CHASTE TREE FRUIT, ARNICA MONTANA WHOLE, GOLD, DIGITALIS, NITROGLYCERIN, VANADIUM
Label structure9 sections

Dosage and administration

Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. If symptoms persist for more than 7 days, consult your health care professional. Consult a physician for use in children under 12 years of age.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

(in each drop): 14.24% of Adonis Vernalis 12X, Agnus Castus 12X, Arnica Montana 12X, Aurum Metallicum 12X, Digitalis Purpurea 12X, Glonoinum 12X, Vanadium Metallicum 12X; 0.10% of Baptisia Tinctoria 3X, Cactus Grandiflorus 3X, Echinacea (Angustifolia) 3X.

INDICATIONS:

OTC - PURPOSE SECTION

May temporarily relieve symptoms of swollen extremities, bruised feeling, cold clammy feet, mild burning pains in leg, and weakness in limbs.**

**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

WARNINGS:

WARNINGS SECTION

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.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. If symptoms persist for more than 7 days, consult your health care professional. Consult a physician for use in children under 12 years of age.

INDICATIONS:

INDICATIONS & USAGE SECTION

May temporarily relieve symptoms of swollen extremities, bruised feeling, cold clammy feet, mild burning pains in leg, and weakness in limbs.**

**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized water, 20% Ethanol.

QUESTIONS:

OTC - QUESTIONS SECTION

Dist. by Energique, Inc.

201 Apple Blvd

Woodbine, IA 51579   800-869-8078

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ENERGIQUE
SINCE 1987
HOMEOPATHIC REMEDY
ARTERIOTONE
1 fl. oz. (30 ml)

ArteriotoneArteriotone

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44911-0230-12024-07-16C16284748780-1ba0f9c33-46da-a910-e053-dadaa90a0b85DRUG FACTS:
44911-0230-12024-01-30C16284748780-1ba0f9c33-46da-a910-e053-dadaa90a0b85DRUG FACTS:
44911-0230-12022-03-09C16284748780-1ba0f9c33-46da-a910-e053-dadaa90a0b85DRUG FACTS:
44911-0230-12021-01-29C16284748780-1ba0f9c33-46da-a910-e053-dadaa90a0b85DRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44911-0230-1Arteriotone30 mL in 1 BOTTLE, DROPPERLIQUID306

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44911-0230ARTERIOTONE (BAPTISIA TINCTORIA, CACTUS GRANDIFLORUS, ECHINACEA (ANGUSTIFOLIA), ADONIS VERNALIS, AGNUS CASTUS, ARNICA MONTANA, AURUM METALLICUM, DIGITALIS PURPUREA, GLONOINUM, VANADIUM METALLICUM) LIQUID [ENERGIQUE, INC.]6Current NDC, Legacy NDC, 1 package rows20240718_4bb46cf1-bfcb-4d57-a982-7ba87e2b299a.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ADONIS VERNALISACTIVE INGREDIENTDX3ZNI25WK1
ARNICA MONTANAACTIVE INGREDIENTO80TY208ZW1
BAPTISIA TINCTORIA ROOTACTIVE INGREDIENT5EF0HWI5WU1
CHASTE TREEACTIVE INGREDIENT433OSF3U8A1
DIGITALISACTIVE INGREDIENTF1T8QT9U8B1
ECHINACEA ANGUSTIFOLIAACTIVE INGREDIENTVB06AV5US81
GOLDACTIVE INGREDIENT79Y1949PYO1
NITROGLYCERINACTIVE INGREDIENTG59M7S0WS31
SELENICEREUS GRANDIFLORUS STEMACTIVE INGREDIENT7114SV0MYK1
VANADIUMACTIVE INGREDIENT00J9J9XKDE1
ADONIS VERNALISACTIVE MOIETYDX3ZNI25WK1
ARNICA MONTANAACTIVE MOIETYO80TY208ZW1
BAPTISIA TINCTORIA ROOTACTIVE MOIETY5EF0HWI5WU1
CHASTE TREEACTIVE MOIETY433OSF3U8A1
DIGITALISACTIVE MOIETYF1T8QT9U8B1
ECHINACEA ANGUSTIFOLIAACTIVE MOIETYVB06AV5US81
GOLDACTIVE MOIETY79Y1949PYO1
NITROGLYCERINACTIVE MOIETYG59M7S0WS31
SELENICEREUS GRANDIFLORUS STEMACTIVE MOIETY7114SV0MYK1
VANADIUMACTIVE MOIETY00J9J9XKDE1
ALCOHOLINACTIVE INGREDIENT3K9958V90M1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44911-023044911-0230-1

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
BAPTISIA TINCTORIA ROOT5EF0HWI5WUACTIB
SELENICEREUS GRANDIFLORUS STEM7114SV0MYKACTIB
ECHINACEA ANGUSTIFOLIA WHOLEVB06AV5US8ACTIB
ADONIS VERNALIS WHOLEDX3ZNI25WKACTIB
CHASTE TREE FRUIT433OSF3U8AACTIB
ARNICA MONTANA WHOLEO80TY208ZWACTIB
GOLD79Y1949PYOACTIB
DIGITALISF1T8QT9U8BACTIB
NITROGLYCERING59M7S0WS3ACTIB
VANADIUM00J9J9XKDEACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 2 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates

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
ArteriotoneBAPTISIA TINCTORIA, CACTUS GRANDIFLORUS, ECHINACEA (ANGUSTIFOLIA), ADONIS VERNALIS, AGNUS CASTUS, ARNICA MONTANA, AURUM METALLICUM, DIGITALIS PURPUREA, GLONOINUM, VANADIUM METALLICUMEnergique, Inc.4bb46cf1-bfcb-4d57-a982-7ba87e2b299a2024-07-16WarningsExact identifier
ndc (package): 44911-0230-1
ndc (product): 44911-0230
ndc11 (package): 44911023001
spl id: 33a86817-1d07-4e87-90c2-11d12edae391
spl set id: 4bb46cf1-bfcb-4d57-a982-7ba87e2b299a

Reported adverse events (FAERS/openFDA)#

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