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Berberis Oxalis

NDC 48951-2161 · Uriel Pharmacy Inc.

Generic nameBerberis Oxalis
Dosage formLIQUID
RouteORAL
Active ingredient(s)BERBERIS VULGARIS ROOT BARK, OXALIS STRICTA WHOLE, SAW PALMETTO, URTICA URENS, VISCUM ALBUM FRUITING TOP, MAGNESIUM SULFATE, UNSPECIFIED FORM, BOS TAURUS PROSTATE GLAND, PENOXSULAM, FERRIC PICRATE
Strength2; 8; 8; 6; 3; 10; 3; 3; 4 [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 classCalculi Dissolution Agent [EPC], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Iron [CS], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Parenteral Iron Replacement [EPC], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
Marketing categoryUNAPPROVED HOMEOPATHIC

Packages

48951-2161-1 — 10 AMPULE in 1 BOX (48951-2161-1) / 1 mL in 1 AMPULE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

44911-0906 — Allium Sativum, Berberis Vulgaris, Fucus Vesiculosus, Phytolacca Decandra, Argentum Metallicum, Aurum Metallicum, Calcarea Fluorica,…, 44911-0907 — Berberis Vulgaris, Cantharis, Causticum, Clematis Erecta, Equisetum Hyemale, Lac Caninum, Lycopodium Clavatum, Mercurius Vivus, Pulsatilla…, 48951-1396 — Amnion Oxalis comp., 48951-1400 — Arnica Nettle, 48951-1401 — Arnica Nettle, 48951-2014 — Bambusa Pulsatilla, 48951-2023 — Bambusa Viscum Stannum, 48951-2054 — Berberis Quartz, 48951-2057 — Berberis Urtica, 48951-2058 — Berberis Viscum, 48951-2162 — Bamboo Rosemary, 48951-4042 — Equisetum Viscum, 48951-6049 — Lycopodium Berberis, 48951-7148 — Oxalis 5, 48951-7214 — Oxalis 1X, 48951-7216 — Magnesium sulf. Bryonia, 48951-7217 — Magnesite Viscum, 48951-7221 — Oxalis 20%, 48951-7224 — Oxalis 5X, 48951-8133 — Renes Veratrum, +521 more

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