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OTC products · Product label record

Lymph Tonic II drug information

ECHINACEA (ANGUSTIFOLIA), COLLINSONIA CANADENSIS, PHYTOLACCA DECANDRA, KALI IODATUM, PINUS SYLVESTRIS, PIX LIQUIDA, FERRUM PHOSPHORICUM, AESCULUS HIPPOCASTANUM, BARYTA CARBONICA, BERBERIS VULGARIS, CALCAREA CARBONICA, CALCAREA PHOSPHORICA, CAUSTICUM, HEPAR SULPHURIS CALCAREUM, KREOSOTUM, LYCOPODIUM CLAVATUM, MERCURIUS SOLUBILIS, NATRUM MURIATICUM, NITRICUM ACIDUM, PHOSPHORUS, PULSATILLA (PRATENSIS), SILICEA, STELLARIA MEDIA, SULPHUR, TEREBINTHINA, THUJA OCCIDENTALIS, BUFO RANA
BioActive Nutritional, Inc. · ORAL

Product NDC: 43857-0658

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Source label information, not individualized medical advice. This record applies to the product and labeler shown below. Compare the exact formulation, strength and country with your package and the current source label.
Generic nameECHINACEA (ANGUSTIFOLIA), COLLINSONIA CANADENSIS, PHYTOLACCA DECANDRA, KALI IODATUM, PINUS SYLVESTRIS, PIX LIQUIDA, FERRUM PHOSPHORICUM, AESCULUS HIPPOCASTANUM, BARYTA CARBONICA, BERBERIS VULGARIS, CALCAREA CARBONICA, CALCAREA PHOSPHORICA, CAUSTICUM, HEPAR SULPHURIS CALCAREUM, KREOSOTUM, LYCOPODIUM CLAVATUM, MERCURIUS SOLUBILIS, NATRUM MURIATICUM, NITRICUM ACIDUM, PHOSPHORUS, PULSATILLA (PRATENSIS), SILICEA, STELLARIA MEDIA, SULPHUR, TEREBINTHINA, THUJA OCCIDENTALIS, BUFO RANA
Labeler / manufacturerBioActive Nutritional, Inc.
RouteORAL
Drug classDrug class not supplied in source label
Product NDC43857-0658
Label effective date2026-09-17

Official product label reference

Lymph Tonic II — BioActive Nutritional, Inc.

This page contains 8 source sections for ECHINACEA (ANGUSTIFOLIA), COLLINSONIA CANADENSIS, PHYTOLACCA DECANDRA, KALI IODATUM, PINUS SYLVESTRIS, PIX LIQUIDA, FERRUM PHOSPHORICUM, AESCULUS HIPPOCASTANUM, BARYTA CARBONICA, BERBERIS VULGARIS, CALCAREA CARBONICA, CALCAREA PHOSPHORICA, CAUSTICUM, HEPAR SULPHURIS CALCAREUM, KREOSOTUM, LYCOPODIUM CLAVATUM, MERCURIUS SOLUBILIS, NATRUM MURIATICUM, NITRICUM ACIDUM, PHOSPHORUS, PULSATILLA (PRATENSIS), SILICEA, STELLARIA MEDIA, SULPHUR, TEREBINTHINA, THUJA OCCIDENTALIS, BUFO RANA, oral route. Label set 0e3265b0-b210-4a4c-80d2-8a9712981d4e, 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

USES: For temporary relief of glandular swelling with inflammation and induration, glands hot, swollen, painful; scrofulous swelling, axillary glands swollen with soreness of the upper arm and tonsils.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Purpose

PURPOSE: Aesculus Hippocastanum - aches,** Baryta Carbonica - headaches,** Berberis Vulgaris - weakness,** Bufo Rana – drainage of lymphatic system,** Calcarea Carbonica - cramps,** Calcarea Phosphorica – minor pains,** Causticum - hoarseness,** Collinsonia Canadensis – dry cough,** Echinacea – sore throat,** Ferrum Phosphoricum - fever,** Hepar Sulphuris Calcareum – swollen joints,** Kali Iodatum – nasal congestion,** Kreosotum – oral health support,** Lycopodium Clavatum – ear pain,** Mercurius Solubilis – runny nose,** Natrum Muriaticum - sneezing,** Nitricum Acidum - weakness,** Phosphorus - stiffness,** Phytolacca Decandra – throat pain,** Pinus Sylvestris – swollen glands,** Pix Liquida - bronchitis,** Pulsatilla – oral health support,** Silicea - analgesic,** Stellaria Media – skin treatment,** Sulphur - itching,** Terebinthina – kidney support,** Thuja Occidentalis – dry cough** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
Dosage and administration — label text
DIRECTIONS: • 10 drops orally, 3 times a day. • Consult a health care professional for use in children under 12 years of age.
Warnings
WARNINGS: Sore Throat Warning Severe or persistent sore throat or sore throat accompanied by high fever, headache, nausea, and vomiting may be serious. Consult physician promptly. Do not use more than 2 days or administer to children under 3 years of age unless directed by a physician. If pregnant or breast-feeding, ask a health care 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: Aesculus Hippocastanum 12X, Baryta Carbonica 12X, Berberis Vulgaris 12X, Bufo Rana 14X, Calcarea Carbonica 12X, Calcarea Phosphorica 12X, Causticum 12X, Collinsonia Canadensis 3X, 12X, Echinacea 3X, Ferrum Phosphoricum 8X, Hepar Sulphuris Calcareum 12X, Kali Iodatum 6X, Kreosotum 12X, Lycopodium Clavatum 12X, Mercurius Solubilis 12X, Natrum Muriaticum 12X, Nitricum Acidum 12X, Phosphorus 12X, Phytolacca Decandra 4X, Pinus Sylvestris 6X, Pix Liquida 6X, Pulsatilla 12X, Silicea 12X, Stellaria Media 12X, Sulphur 12X, Terebinthina 12X, Thuja Occidentalis 12X.
Child safety
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, 25% Ethanol
Questions
QUESTIONS: Distributed by: BioActive Nutritional, Inc. 1803 N. Wickham Rd. Melbourne, FL 32935 bioactivenutritional.com 1-800-288-9525

Official sources and product identifiers

Substances listed: ECHINACEA ANGUSTIFOLIA WHOLE, COLLINSONIA CANADENSIS ROOT, PHYTOLACCA AMERICANA ROOT, POTASSIUM IODIDE, PINUS SYLVESTRIS LEAFY TWIG, PINE TAR, FERROSOFERRIC PHOSPHATE, HORSE CHESTNUT, BARIUM CARBONATE, BERBERIS VULGARIS ROOT BARK, OYSTER SHELL CALCIUM CARBONATE, CRUDE, TRIBASIC CALCIUM PHOSPHATE, CAUSTICUM, CALCIUM SULFIDE, WOOD CREOSOTE, LYCOPODIUM CLAVATUM SPORE, MERCURIUS SOLUBILIS, SODIUM CHLORIDE, NITRIC ACID, PHOSPHORUS, PULSATILLA PRATENSIS WHOLE, SILICON DIOXIDE, STELLARIA MEDIA, SULFUR, TURPENTINE OIL, THUJA OCCIDENTALIS LEAFY TWIG, BUFO BUFO CUTANEOUS GLAND

Package NDC codes

43857-0658-1

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.