Betula Argentum

FDA Drug Profile — Betula Argentum

Betula Argentum is listed in the FDA National Drug Code directory with 1 NDC code, marketed under brand name including Betula Argentum. Available dosage form: liquid.

Drug Details

Generic Name
Betula Argentum
Brand Names
Betula Argentum
Application Number
Sponsor
Uriel Pharmacy Inc.
NDC Codes
1
Dosage Forms
LIQUID
Routes
ORAL
Active Ingredients
APIS MELLIFERA, BETULA PUBESCENS BARK, BETULA PUBESCENS LEAF, FORMICA RUFA, SILVER, ARNICA MONTANA

Indications and Usage

Directions: FOR ORAL USE.

Warnings

Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use.