Heartex

Manufacturer
Energique, Inc. | Apotheca Company
Effective date
2022-05-23
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:00:43

Label at a glance#

ProductHeartex
Active ingredientSPONGIA OFFICINALIS SKELETON, ROASTED, GINKGO, DIGITALIS, ACONITUM NAPELLUS, PORK HEART, PORK KIDNEY, PORK INTESTINE, GERMANIUM SESQUIOXIDE, COBALT, MANGANESE, OXOGLURIC ACID, ANHYDROUS CITRIC ACID, FUMARIC ACID, MALIC ACID, 1,4-NAPHTHOQUINONE, SODIUM PYRUVATE, SUCCINIC ACID, ARSENIC, GOLD, ACONITIC ACID, (Z)-, SELENICEREUS GRANDIFLORUS STEM, PHOSPHORUS
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, 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

Spongia Tosta 3X, 6X, 12X, Ginkgo Biloba 6X, Digitalis Purpurea 6X, 12X, Aconitum Napellus 6X, 12X, 30X, Heart (Suis) 6X, 12X, 30X, Kidney (Suis) 6X, 12X, 30X, Small Intestine (Suis) 6X, 12X, 30X, Germanium Sesquioxide 8X, Cobaltum Metallicum 8X, 12X, Manganum Metallicum 8X, 12X, Alpha-Ketoglutaricum Acidum 8X, 12X, 30X, Citricum Acidum 8X, 12X, 30X, Fumaricum Acidum 8X, 12X, 30X, Malicum Acidum 8X, 12X, 30X, Naphthochinonum 8X, 12X, 30X, Natrum Pyruvicum 8X, 12X, 30X, Succinicum Acidum 8X, 12X, 30X, Arsenicum Metallicum 12X, Aurum Metallicum 12X, Aconiticum Acidum Cis 12X, 30X, Cactus Grandiflorus 12X, 30X, Phosphorus 12X, 30X

INDICATIONS:

OTC - PURPOSE SECTION

Heart, Small Intestine support.**

**These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

WARNINGS:

WARNINGS SECTION

If pregnant or breastfeeding, 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

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

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

INDICATIONS:

INDICATIONS & USAGE SECTION

Heart, Small Intestine support.**

**These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized water, 20% Ethanol.

QUESTONS:

OTC - QUESTIONS SECTION

Dist. by Energique, Inc.
201 Apple Blvd.
Woodbine, IA 51579   800.868.8078

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ENERGIQUE

SINCE 1987

HOMEOPATHIC REMEDY

HEARTEX III

1 fl. oz. (30 ml)

Heartex IIIHeartex III

Products#

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

DailyMed product names page 1 of 1 · 28 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44911-035144911-0351-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 24 matching rows.

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
b7f9923e-ac59-4b8f-97c5-5f75f71ba17eb42a3d11-e822-4c0b-a23a-9d28dfc220ed2022-05-23WarningsExact identifier
spl id: b7f9923e-ac59-4b8f-97c5-5f75f71ba17e
spl set id: b42a3d11-e822-4c0b-a23a-9d28dfc220ed

Reported adverse events (FAERS/openFDA)#

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