Berberis Oxalis

FDA Drug Profile — Berberis Oxalis

Berberis Oxalis is listed in the FDA National Drug Code directory with 2 NDC codes, marketed under brand name including Berberis Oxalis. Available dosage form: liquid.

Drug Details

Generic Name
Berberis Oxalis
Brand Names
Berberis Oxalis
Application Number
Sponsor
Uriel Pharmacy Inc.
NDC Codes
2
Dosage Forms
LIQUID
Routes
ORAL
Active Ingredients
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

Indications and Usage

FOR ORAL USE ONLY

Warnings

Warnings: NOT FOR INJECTION Do not use if allergic to any ingredient. Contains traces of lactose. Consult a physician if symptoms worsen. If pregnant or nursing, consult a physician before use. Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated