Vertigo Syncope Drops

FDA Drug Profile — Vertigo Syncope Drops 2115

Vertigo Syncope Drops is listed in the FDA National Drug Code directory with 1 NDC code, marketed under brand name including Vertigo Syncope Drops 2115. Available dosage form: liquid.

Drug Details

Generic Name
Vertigo Syncope Drops
Brand Names
Vertigo Syncope Drops 2115
Application Number
Sponsor
Professional Complementary Health Formulas
NDC Codes
1
Dosage Forms
LIQUID
Routes
ORAL
Active Ingredients
ARNICA MONTANA WHOLE, CENTELLA ASIATICA LEAF, PHOSPHORIC ACID, AMBERGRIS, SILVER NITRATE, ANAMIRTA COCCULUS FRUIT, CONIUM MACULATUM FLOWERING TOP, CANIS LUPUS FAMILIARIS MILK, THERIDION CURASSAVICUM

Indications and Usage

INDICATIONS For temporary relief of occasional dizziness or lightheadedness, loss of balance, nausea, or vomiting.*

Warnings

WARNINGS Persistent symptoms may be a sign of a serious condition. If symptoms persist or are accompanied by a fever, persistent headache, stiff neck, or changes in vision or hearing, consult a doctor. Keep out of the reach of children. In case of overdose, get medical help or contact a poison control center right away. If pregnant or breastfeeding, ask a healthcare professional before use. Keep out of the reach of children. If pregnant or breastfeeding, ask a healthcare professional before use.