Berberis Oxalis

Product NDC

48951-2161

11-digit product format

489512161

Labeler code

48951

Product ID

48951-2161_3638612f-227f-2224-e063-6394a90a05b6

Type

HUMAN OTC DRUG

Nonproprietary name

Berberis Oxalis

Dosage form

LIQUID

Route

ORAL

Labeler

Uriel Pharmacy Inc.

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

2009-09-01

Substance

BERBERIS VULGARIS ROOT BARK; BOS TAURUS PROSTATE GLAND; FERRIC PICRATE; MAGNESIUM SULFATE, UNSPECIFIED FORM; OXALIS STRICTA WHOLE; PENOXSULAM; SAW PALMETTO; URTICA URENS; VISCUM ALBUM FRUITING TOP

Active strength

2; 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 classes

Calculi 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]

NDC exclude flag

No

Listing certified through

2026-12-31

Current FDA listing

Yes