Cardiac Care-Adjunctive Complex

Manufacturer
Newton Laboratories, Inc.
Effective date
2019-11-15
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:01:04

Label at a glance#

ProductCardiac Care-Adjunctive Complex
Active ingredientPOTASSIUM IODIDE, LACHESIS MUTA VENOM, LYCOPUS VIRGINICUS, NAJA NAJA VENOM, STRYCHNOS NUX-VOMICA SEED, PHOSPHORUS, PULSATILLA VULGARIS, MICRURUS CORALLINUS VENOM, ACONITUM NAPELLUS, ARSENIC TRIOXIDE, GOLD, BARIUM CARBONATE, BENZOIC ACID, BERBERIS VULGARIS ROOT BARK, BRYONIA ALBA ROOT, CALCIUM FLUORIDE, LYTTA VESICATORIA, CEANOTHUS AMERICANUS LEAF, CHELIDONIUM MAJUS, CHIONANTHUS VIRGINICUS BARK, CONVALLARIA MAJALIS, CROTALUS HORRIDUS HORRIDUS VENOM, DIGITALIS, HYDROFLUORIC ACID, GELSEMIUM SEMPERVIRENS ROOT, NITROGLYCERIN, TOXICODENDRON PUBESCENS LEAF, VIPERA BERUS VENOM, ECHINACEA, UNSPECIFIED, HYPERICUM PERFORATUM, VALERIAN, CINCHONA OFFICINALIS BARK
Label structure9 sections

Label contents#

Full prescribing information#

PREGNANCY OR BREAST FEEDING SECTION

OTC - PREGNANCY OR BREAST FEEDING SECTION

If ​pregnant or breast-feeding, ​ask a doctor before use.

WARNINGS SECTION

Warning:​Keep out of reach of children. Do not use​ if tamper-evident seal is broken or missing. If symptoms worsen or persist for more than a few days, consult a doctor. If ​pregnant or breast-feeding,​ ask a doctor before use.

QUESTIONS? SECTION

OTC - QUESTIONS SECTION

newtonlabs.net – Questions? 800.448.7256

Newton Laboratories, Inc. FDA Est # 1051203 - Conyers, GA 30013

INACTIVE INGREDIENT SECTION

Inactive Ingredients: USP Purified Water; USP Gluten-free, non-GMO, organic cane alcohol 20%.

PURPOSE SECTION

ABUSE SECTION

Formulated for symptoms associated with arteriosclerosis, tachycardia, arrhythmias, palpitations and other related conditions.

ACTIVE INGREDIENT SECTION

OTC - ACTIVE INGREDIENT SECTION

Equal parts of Echinacea 6x, Hypericum perforatum 6x, Valeriana officinalis 6x, Aconitum napellus 15x, Arsenicum album 15x, Aurum metallicum 15x, Baryta carbonica 15x, Benzoicum acidum 15x, Berberis vulgaris 15x, Bryonia 15x, Calcarea fluorica 15x, Cantharis 15x, Ceanothus americanus 15x, Chelidonium majus 15x, Chionanthus virginica 15x, Cinchona officinalis 15x, Convallaria majalis 15x, Crotalus horridus 15x, Digitalis purpurea 15x, Gelsemium sempervirens 15x, Glonoinum 15x, Hydrofluoricum acidum 15x, Kali iodatum 15x, Lachesis mutus 15x, Lycopus virginicus 15x, Naja tripudians 15x, Nux vomica 15x, Phosphorus 15x, Pulsatilla 15x, Rhus toxicodendron 15x, Vipera berus 15x, Elaps corallinus 30x.

DOSAGE & ADMINISTRATION SECTION

Directions:. Adults, take 6 drops by mouth one to four times daily or as directed by a health professional.

INDICATIONS & USAGE SECTION

Formulated for symptoms associated with arteriosclerosis, tachycardia, arrhythmias, palpitations and other related conditions.

PACKAGE LABEL.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package LabelPackage Label

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55714-465055714-4650-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 34 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.

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Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
b67444b2-70bb-66a4-e053-2995a90a6a0897695c98-3f8a-a751-e053-2995a90afa142020-12-14WarningsExact identifier
spl set id: 97695c98-3f8a-a751-e053-2995a90afa14

Reported adverse events (FAERS/openFDA)#

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