Aesculus Combination

FDA Drug Profile — Aesculus Combination 9202

Aesculus Combination is listed in the FDA National Drug Code directory with 1 NDC code, marketed under brand name including Aesculus Combination 9202. Available dosage form: liquid.

Drug Details

Generic Name
Aesculus Combination
Brand Names
Aesculus Combination 9202
Application Number
Sponsor
Professional Complementary Health Formulas
NDC Codes
1
Dosage Forms
LIQUID
Routes
ORAL
Active Ingredients
HORSE CHESTNUT, ECHINACEA ANGUSTIFOLIA WHOLE, ARNICA MONTANA WHOLE, CLAVICEPS PURPUREA SCLEROTIUM, AVISCUMINE, APIS MELLIFERA, BAPTISIA TINCTORIA WHOLE, BENZOIC ACID, COLCHICUM AUTUMNALE BULB, HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK, RUTA GRAVEOLENS FLOWERING TOP, BARIUM IODIDE, EUPATORIUM PERFOLIATUM FLOWERING TOP, TOXICODENDRON PUBESCENS LEAF, SOLANUM NIGRUM TOP, SODIUM PYRUVATE, BEEF HEART, TOBACCO LEAF, COPPER, SULFUR

Indications and Usage

INDICATIONS For the temporary relief of occasional constipation, sluggish digestion, minor joint pain or swelling, or sporadic leg pain, particularly when walking.*

Warnings

WARNINGS In case of overdose, get medical help or contact a poison control center right away. Keep out of the reach of children. If pregnant or breastfeeding, ask a healthcare professional before use.