Helleborus comp. A

FDA Drug Profile — Helleborus comp. A

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

Drug Details

Generic Name
Helleborus comp. A
Brand Names
Helleborus comp. A
Application Number
Sponsor
Uriel Pharmacy Inc.
NDC Codes
1
Dosage Forms
LIQUID
Routes
ORAL
Active Ingredients
TIN, PHOSPHORUS, ARSENIC TRIOXIDE, LEAD MONOSILICATE, SILVER, FORMICA RUFA, ANTIMONY, HELLEBORUS NIGER ROOT, POTASSIUM PHOSPHATE, MONOBASIC, JUGLANS REGIA LEAF

Indications and Usage

FOR ORAL USE ONLY

Warnings

Warnings: NOT FOR INJECTION Do not use if allergic to any ingredient. Contains traces of lactose. Consult a physician if symptoms worsen. If pregnant or nursing, consult a physician before use. Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.