Aconitum e tub. 30

FDA Drug Profile — Aconitum e tub. 30

Aconitum e tub. 30 is listed in the FDA National Drug Code directory with 1 NDC code, marketed under brand name including Aconitum e tub. 30. Available dosage form: liquid.

Drug Details

Generic Name
Aconitum e tub. 30
Brand Names
Aconitum e tub. 30
Application Number
Sponsor
Uriel Pharmacy Inc.
NDC Codes
1
Dosage Forms
LIQUID
Routes
ORAL
Active Ingredients
ACONITUM NAPELLUS

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.