Aconitum napellus

FDA Drug Profile — Aconitum napellus, Arnica montana, Aconitum napellus 7101, ACONITE

Drug Details

Generic Name
Aconitum napellus
Brand Names
Aconitum napellus, Arnica montana, Aconitum napellus 7101, ACONITE
Application Number
Sponsor
Hahnemann Laboratories, Inc.
NDC Codes
33
Dosage Forms
PELLET, LIQUID
Routes
ORAL
Active Ingredients
ACONITUM NAPELLUS, ARNICA MONTANA, ACONITUM NAPELLUS WHOLE

Indications and Usage

INDICATIONS Condition listed above or as directed by the physician

Warnings

WARNINGS This product is to be used for self-limiting conditions If symptoms do not improve in 4 days, or worsen, discontinue use and seek assistance of health professional As with any drug, if you are preganant, or nursing a baby, seek professional advice before taking this product Keep this and all medication out of reach of children Do not use if capseal is broken or missing. Close the cap tightly after use.