Cardiac Care

Manufacturer
Newton Laboratories, Inc.
Effective date
2017-12-13
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:08:42

Label at a glance#

ProductCardiac Care
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 structure10 sections

Label contents#

Full prescribing information#

KEEP OUT OF REACH OF CHILDREN SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

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

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

Questions? 1.800.448.7256

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 3x, Hypericum 3x,Valeriana 3x, Aconitum nap. 10x, Arsenicum alb. 10x, Aur. met.10x, Baryta carb. 10x, Benzoicum acidum 10x, Berber. vulg. 10x, Bryonia 10x, Calc. fluor. 10x, Cantharis 10x, Ceanothus 10x, Chelidonium majus 10x, Chionanthus virginica 10x, Cinchona 10x, Convallaria 10x, Crotalus horridus 10x, Digitalis 10x, Gelsemium 10x, Glonoinum 10x, Hydroflouricum acidum 10x, Kali iod.10x, Lachesis 10x, Lycopus virginicus 10x, Naja 10x, Nux vom. 10x, Phosphorus 10x, Pulsatilla 10x, Rhus toxicodendron 10x, Vipera berus 10x, 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

CARDIAC Care 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
55714-464055714-4640-1, 55714-4640-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 33 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
96b52194-8e01-bf94-e053-2a95a90a08a760406a32-9fd1-a4bb-e053-2a91aa0afd422019-11-06WarningsExact identifier
spl set id: 60406a32-9fd1-a4bb-e053-2a91aa0afd42

Reported adverse events (FAERS/openFDA)#

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