Hamamelis Aesculus

FDA Drug Profile — Hamamelis Aesculus

Hamamelis Aesculus is listed in the FDA National Drug Code directory with 2 NDC codes, marketed under brand name including Hamamelis Aesculus. Available dosage forms: liquid, pellet.

Drug Details

Generic Name
Hamamelis Aesculus
Brand Names
Hamamelis Aesculus
Application Number
Sponsor
Uriel Pharmacy Inc.
NDC Codes
2
Dosage Forms
LIQUID, PELLET
Routes
ORAL
Active Ingredients
HORSE CHESTNUT, HAMAMELIS VIRGINIANA TOP, PAEONIA OFFICINALIS ROOT, PULSATILLA VULGARIS, HIRUDIN, MERCURY, AESCULUS GLABRA NUT, HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK, DESIRUDIN

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.