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Aller-Chord A

NDC 64578-0057 · Energetix Corporation

Generic nameAlfalfa, Allium Cepa, Ambrosia Artemisiaefolia, Bryonia (Alba), Citricum Acidum, Coumarinum, Euphrasia Officinalis, Glandula Suprarenalis Suis, Hepar Suis, Histaminum Hydrochloricum, Hydrastis Canadensis, Juniperus Communis, Mucosa Nasalis Suis, Natrum Sulphuricum, Phosphorus, Pothos Foetidus, Pulsatilla (Vulgaris), Solidago Virgaurea, Sulphur, Tanacetum Vulgare, Taraxacum Officinale, Trifolium Pratense
Dosage formLIQUID
RouteORAL
Active ingredient(s)PULSATILLA VULGARIS, SOLIDAGO VIRGAUREA FLOWERING TOP, SULFUR, TANACETUM VULGARE TOP, TARAXACUM OFFICINALE, TRIFOLIUM PRATENSE FLOWER, ALFALFA, ONION, AMBROSIA ARTEMISIIFOLIA, BRYONIA ALBA ROOT, ANHYDROUS CITRIC ACID, COUMARIN, EUPHRASIA STRICTA, SUS SCROFA ADRENAL GLAND, PORK LIVER, HISTAMINE DIHYDROCHLORIDE, GOLDENSEAL, JUNIPER BERRY, SUS SCROFA NASAL MUCOSA, SODIUM SULFATE, PHOSPHORUS, SYMPLOCARPUS FOETIDUS ROOT
Strength9; 6; 12; 6; 12; 6; 9; 12; 9; 6; 12; 9; 12; 12; 9; 12; 9; 9; 9; 9; 9; 9 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmacologic classAcidifying Activity [MoA], Allergens [CS], Allergens [CS], Anti-coagulant [EPC], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Decreased Coagulation Factor Activity [PE], Dietary Proteins [CS], Dietary Proteins [CS], Food Additives [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Vegetable Proteins [CS]
Marketing categoryUNAPPROVED HOMEOPATHIC

Packages

64578-0057-1 — 59.1 mL in 1 BOTTLE, DROPPER (64578-0057-1)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

63629-9259 — SULFACETAMIDE SODIUM, SULFUR, 63629-9260 — SULFACETAMIDE SODIUM, SULFUR, 63629-9261 — SULFACETAMIDE SODIUM, SULFUR, 63750-006 — SULFUR, 63868-229 — Aspirin, Citric Acid, Sodium Bicarbonate, 63868-569 — Aspirin, Anhydrous Citric Acid, Sodium Bicarbonate, 63868-604 — MATRICARIA CHAMOMILLA WHOLE, MERCURIUS SOLUBILIS, SULFUR, 63941-421 — Aspirin, Citric Acid, Sodium Bicarbonate, 64380-116 — Sodium Sulfate, Potassium Sulfate and Magnesium Sulfate Oral, 64471-196 — Euphrasia Officinalis, Kali Iodatum, Sabadilla, Sticta Pulmonaria, Histaminum Hydrochloricum, Quercetin, Succinicum Acidum, Ambrosia Artemisiaefolia, 64578-0058 — Absinthium, Baptisia Tinctoria, Cajuputum, Capsicum Annuum, Cinchona Officinalis, Fragaria Vesca, Gentiana Lutea, Glandula Suprarenalis Suis, Hepar Suis, Lycopodium Clavatum, Mucosa Nasalis Suis, Nux Vomica, Pancreas Suis, Pulsatilla, Pyrogenium, Quassia, Senna, Triticum Repens, 64578-0060 — Homeopathic Liquid, 64578-0061 — Homeopathic Liquid, 64578-0063 — Homeopathic Liquid, 64578-0065 — Baptisia Tinctoria, Ceanothus Americanus, Citricum Acidum, Echinacea (Angustifolia), Gelsemium Sempervirens, Hydrocotyle Asiatica, Lycopodium Clavatum, Mercurius Solubilis, Mezereum, Morbillinum, Nux Vomica, Paloondo, Phytolacca Decandra, Sepia, Thuja Occidentalis, Thyroidinum (Bovine), 64578-0068 — Allium Cepa, Allium Sativum, Alpha-Lipoicum Acidum, Alumina, Arsenicum Metallicum, Berberis Vulgaris, Cadmium Metallicum, Carduus Marianus, Cetraria Islandica, Cuprum Metallicum, Cysteinum, Glycyrrhiza Glabra, Hepar Suis, Lappa Major, Lycopodium Clavatum, Mercurius Solubilis, Nux Vomica, Plantago Major, Plumbum Metallicum, Pyridoxinum Hydrochloricum, Selenium Metallicum, Stillingia Sylvatica, Thyroidinum, Trifolium Pratense, Zingiber Officinale, 64578-0073 — Homeopathic Liquid, 64578-0075 — Homeopathic Liquid, 64578-0076 — Homeopathic Liquid, 64578-0083 — Aconitum Napellus, Belladonna, Bryonia (Alba), Chamomilla, +2747 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.