Rhus Aconitum

NDC 48951-8142 · Uriel Pharmacy Inc.

Generic nameRhus Aconitum

Dosage formPELLET

RouteORAL

Active ingredient(s)GELSEMIUM SEMPERVIRENS ROOT, ACONITUM NAPELLUS, PSEUDOGNAPHALIUM LUTEOALBUM LEAF, MANDRAGORA OFFICINARUM ROOT, TOXICODENDRON PUBESCENS LEAF, ATROPA BELLADONNA, PENOXSULAM

Strength4; 6; 3; 4; 10; 4; 4 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1

Marketing categoryUNAPPROVED HOMEOPATHIC

Packages

48951-8142-2 — 1350 PELLET in 1 BOTTLE, GLASS (48951-8142-2)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

48951-3260 — Cartilago Argentum, 48951-5027 — Gnaphalium Stannum, 48951-6012 — Lachesis Belladonna, 48951-6021 — Lavender Quartz Ear Oil, 48951-7015 — Mandragora Rheum, 48951-7213 — Olibanum Belladonna comp., 48951-7222 — Melissa, 48951-8084 — Pulmo Bryonia, 48951-8086 — Pulmo Echinacea, 48951-8140 — Rhus Aconitum, 48951-8189 — Silicea Belladonna, 48951-8390 — Plantain Spruce Cough, 48951-9061 — Viscum Belladonna, 50181-0065 — Apis Mellifica, Arnica Montana, Berberis Vulgaris, Gelsemium Sempervirens, Solidago Virgaurea, Phytolacca Decandra, Hydrastis Canadensis,…, 50181-0071 — Spongia Tosta, Iodium, Fucus Vesiculosus, Belladonna, Adenosinum Triphosphoricum Dinatrum, Parathyroid Gland (Bovine), Selenium Metallicum,…, 50181-0080 — Eschscholtzia Californica, Chamomilla, Cina, Coffea Cruda, Nux Vomica, Passiflora Incarnata, Pulsatilla (Pratensis), Ignatia Amara, Kali…, 50181-0082 — Arnica Montana, Hypericum Perforatum, Plantago Major, Aconitum Napellus, Mercurius Solubilis, Hekla Lava, Argentum Nitricum, Belladonna,…, 50845-0237 — Aconitum Napellus, Arnica Montana, Belladonna, Cimicifuga Racemosa, Euphorbium Officinarum, Gelsemium Sempervirens, Gnaphalium…, 50845-0247 — Anas Barbariae, Hepatis Et Cordis Extractum, Antimonium Tartaricum, Apis Mellifica, Baptisia Tinctoria, Bryonia (Alba), Eupatorium…, 50845-0270 — Allium Cepa, Apis Mellifica, Aralia Racemosa, Arundo Mauritanica, Baptisia Tinctoria, Echinacea (Angustifolia), Euphrasia Officinalis,…, +989 more

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