Helleborus e pl. tota 4

FDA Drug Profile — Helleborus e pl. tota 4

Helleborus e pl. tota 4 is listed in the FDA National Drug Code directory with 1 NDC code, marketed under brand name including Helleborus e pl. tota 4. Available dosage form: liquid.

Drug Details

Generic Name
Helleborus e pl. tota 4
Brand Names
Helleborus e pl. tota 4
Application Number
Sponsor
Uriel Pharmacy Inc.
NDC Codes
1
Dosage Forms
LIQUID
Routes
ORAL
Active Ingredients
HELLEBORUS FOETIDUS ROOT

Indications and Usage

FOR ORAL USE ONLY

Warnings

Warnings: NOT FOR INJECTION Do not use if allergic to any ingredient. 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.