Arnica Betula B

FDA Drug Profile — Arnica Betula B

Arnica Betula B is listed in the FDA National Drug Code directory with 2 NDC codes, marketed under brand name including Arnica Betula B. Available dosage forms: liquid, pellet.

Drug Details

Generic Name
Arnica Betula B
Brand Names
Arnica Betula B
Application Number
Sponsor
Uriel Pharmacy Inc.
NDC Codes
2
Dosage Forms
LIQUID, PELLET
Routes
ORAL
Active Ingredients
BETULA PUBESCENS LEAF, BETULA PUBESCENS BARK, BOS TAURUS CEREBELLUM, BOS TAURUS BRAIN, BOS TAURUS PINEAL GLAND, SUS SCROFA EAR, BOS TAURUS NERVE, ARNICA MONTANA, LEAD, FORMICA RUFA, BIFENTHRIN, BOS TAURUS MESENCEPHALON, HONEY

Indications and Usage

Directions: FOR ORAL USE ONLY.

Warnings

Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Contains sugar. Diabetics and persons intolerant of sucrose (sugar): Consult a doctor before use. 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. Do not use if safety seal is broken or missing.