Helleborus e pl. tota 12
Helleborus e pl. tota 12 is listed in the FDA National Drug Code directory with 1 NDC code, marketed under brand name including Helleborus e pl. tota 12. Available dosage form: liquid.
Drug Details
- Generic Name
- Helleborus e pl. tota 12
- Brand Names
- Helleborus e pl. tota 12
- Application Number
- Sponsor
- Uriel Pharmacy Inc.
- NDC Codes
- 1
- Dosage Forms
- LIQUID
- Routes
- ORAL
- Active Ingredients
- HELLEBORUS FOETIDUS ROOT
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.