Achillea millefolium

FDA Drug Profile — Unda 1

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

Drug Details

Generic Name
Achillea millefolium
Brand Names
Unda 1
Application Number
Sponsor
Seroyal USA
NDC Codes
1
Dosage Forms
LIQUID
Routes
ORAL
Active Ingredients
ACHILLEA MILLEFOLIUM, ARCTOSTAPHYLOS UVA-URSI LEAF, VALERIAN, ANGELICA ARCHANGELICA ROOT, EQUISETUM ARVENSE TOP, LYCOPODIUM CLAVATUM SPORE, LARIX DECIDUA RESIN, SILVER

Indications and Usage

Take 15 minutes before meals.

Warnings

WARNINGS Stop use and ask doctor if symptoms worsen or persist more than 5 days. If pregnant or breast-feeding ask a health care professional before use. Keep out of reach of children. In case of accidental overdose, seek professional assistance or contact a poison control center immediately Contains ethyl alcohol 30%