Aconitum napellus

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

Aconitum napellus is listed in the FDA National Drug Code directory with 33 NDC codes, marketed under brand names including Aconitum napellus, Aconitum napellus 7101, ACONITE. Available dosage forms: pellet, liquid.

Drug Details

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

Indications and Usage

INDICATIONS: May temporarily relieve fever, irritated throat, and acute irritation of the bladder.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Warnings

WARNINGS: If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Do not use if tamper evident seal is broken or missing. Store in a cool, dry place. Warning: Severe or persistent sore throat or sore throat accompanied by high fever, headache, nausea, and vomiting may be serious. Consult physician promptly. Do not use more than 2 days or administer to children under 3 years of age unless directed by a physician.