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Prescription products · Product label record

Lymphastat drug information

BAPTISIA TINCTORIA, ECHINACEA (ANGUSTIFOLIA), LOBELIA INFLATA, LOMATIUM DISSECTUM, HYDRASTIS CANADENSIS, LUNG (SUIS), PHYTOLACCA DECANDRA, SYMPHYTUM OFFICINALE, ACONITUM NAPELLUS, ARSENICUM ALBUM, BELLADONNA, BRYONIA (ALBA), CAUSTICUM, EUPATORIUM PERFOLIATUM, FERRUM PHOSPHORICUM, GELSEMIUM SEMPERVIRENS, HYPERICUM PERFORATUM, KALI CARBONICUM, LACHESIS MUTUS, NATRUM SULPHURICUM, PHOSPHORUS, PULSATILLA (PRATENSIS), RHUS TOX, SILICEA, SULPHUR, PYROGENIUM
Energique, Inc. · ORAL

Product NDC: 44911-0615

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Generic nameBAPTISIA TINCTORIA, ECHINACEA (ANGUSTIFOLIA), LOBELIA INFLATA, LOMATIUM DISSECTUM, HYDRASTIS CANADENSIS, LUNG (SUIS), PHYTOLACCA DECANDRA, SYMPHYTUM OFFICINALE, ACONITUM NAPELLUS, ARSENICUM ALBUM, BELLADONNA, BRYONIA (ALBA), CAUSTICUM, EUPATORIUM PERFOLIATUM, FERRUM PHOSPHORICUM, GELSEMIUM SEMPERVIRENS, HYPERICUM PERFORATUM, KALI CARBONICUM, LACHESIS MUTUS, NATRUM SULPHURICUM, PHOSPHORUS, PULSATILLA (PRATENSIS), RHUS TOX, SILICEA, SULPHUR, PYROGENIUM
Labeler / manufacturerEnergique, Inc.
RouteORAL
Drug classDrug class not supplied in source label
Product NDC44911-0615
Label effective date2024-10-28

Official product label reference

Lymphastat — Energique, Inc.

This page contains 8 source sections for BAPTISIA TINCTORIA, ECHINACEA (ANGUSTIFOLIA), LOBELIA INFLATA, LOMATIUM DISSECTUM, HYDRASTIS CANADENSIS, LUNG (SUIS), PHYTOLACCA DECANDRA, SYMPHYTUM OFFICINALE, ACONITUM NAPELLUS, ARSENICUM ALBUM, BELLADONNA, BRYONIA (ALBA), CAUSTICUM, EUPATORIUM PERFOLIATUM, FERRUM PHOSPHORICUM, GELSEMIUM SEMPERVIRENS, HYPERICUM PERFORATUM, KALI CARBONICUM, LACHESIS MUTUS, NATRUM SULPHURICUM, PHOSPHORUS, PULSATILLA (PRATENSIS), RHUS TOX, SILICEA, SULPHUR, PYROGENIUM, oral route. Label set ed3e0362-a4d3-46fa-a045-17bf659b777c, version 2.

Retrieved 2026-10-02 · openFDA dataset updated 2026-10-02 · Check the current DailyMed label

Label records can cover multiple strengths or package sizes. A label listing does not by itself establish FDA approval or current market availability. Check the source and application history for this specific product.

Uses described in the label

INDICATIONS: May temporarily relieve symptoms associated with viral and bacterial infections, such as fever, irritated throat, and cough with tickle in the throat.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Purpose

INDICATIONS: May temporarily relieve symptoms associated with viral and bacterial infections, such as fever, irritated throat, and cough with tickle in the throat.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
Dosage and administration — label text
DIRECTIONS: 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 2 days, consult your health care professional. Consult a physician for use in children under 12 years of age.
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.
Active ingredient
ACTIVE INGREDIENTS: (in each drop): 4.53% of Hydrastis Canadensis 6X, Lung (Suis) 6X, Phytolacca Decandra 6X, Symphytum Officinale 6X; Aconitum Napellus 12X, Arsenicum Album 12X, Belladonna 12X, Bryonia 12X, Causticum 12X, Eupatorium Perfoliatum 12X, Ferrum Phosphoricum 12X, Gelsemium Sempervirens 12X, Hypericum Perforatum 12X, Kali Carbonicum 12X, Lachesis Mutus 12X, Natrum Sulphuricum 12X, Phosphorus 12X, Pulsatilla (Pratensis) 12X, Rhus Tox 12X, Silicea 12X, Sulphur 12X; Pyrogenium 30X. 0.10% of Baptisia Tinctoria 3X, Echinacea (Angustifolia) 3X, Lobelia Inflata 3X, Lomatium Dissectum 3X.
Child safety
KEEP OUT OF REACH OF CHILDREN: Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
Inactive ingredient
INACTIVE INGREDIENTS: Demineralized water, 20% Ethanol.
Questions
QUESTIONS: Dist. by Energique, Inc. 201 Apple Blvd Woodbine, IA 51579 800.869.8078

Official sources and product identifiers

Substances listed: BAPTISIA TINCTORIA ROOT, ECHINACEA ANGUSTIFOLIA WHOLE, LOBELIA INFLATA WHOLE, LOMATIUM DISSECTUM ROOT, GOLDENSEAL, SUS SCROFA LUNG, PHYTOLACCA AMERICANA ROOT, COMFREY ROOT, ACONITUM NAPELLUS WHOLE, ARSENIC TRIOXIDE, ATROPA BELLADONNA, BRYONIA ALBA ROOT, CAUSTICUM, EUPATORIUM PERFOLIATUM FLOWERING TOP, FERROSOFERRIC PHOSPHATE, GELSEMIUM SEMPERVIRENS ROOT, HYPERICUM PERFORATUM WHOLE, POTASSIUM CARBONATE, LACHESIS MUTA VENOM, SODIUM SULFATE, PHOSPHORUS, PULSATILLA PRATENSIS WHOLE, TOXICODENDRON PUBESCENS LEAF, SILICON DIOXIDE, SULFUR, RANCID BEEF

Package NDC codes

44911-0615-1

Further research and background

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Coverage and corrections

The text is extracted from a US structured product label. Tables are represented as text where supplied; formatting and illustrations may be lost. A missing section does not mean a risk is absent. This reference has not been independently reviewed by a clinician and is not a live safety-alert service.

Source retrieved 2026-10-02. Read the source policy.