Rhus Aconitum
Rhus Aconitum is listed in the FDA National Drug Code directory with 2 NDC codes, marketed under brand name including Rhus Aconitum. Available dosage forms: liquid, pellet.
Drug Details
- Generic Name
- Rhus Aconitum
- Brand Names
- Rhus Aconitum
- Application Number
- Sponsor
- Uriel Pharmacy Inc.
- NDC Codes
- 2
- Dosage Forms
- LIQUID, PELLET
- Routes
- ORAL
- Active Ingredients
- GELSEMIUM SEMPERVIRENS ROOT, PSEUDOGNAPHALIUM LUTEOALBUM LEAF, ACONITUM NAPELLUS, ATROPA BELLADONNA, MANDRAGORA OFFICINARUM ROOT, TOXICODENDRON PUBESCENS LEAF, PENOXSULAM
Indications and Usage
Directions: FOR ORAL USE ONLY.
Warnings
Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Contains sugar. Diabetics and persons intolerant of sucrose (sugar): Consult a doctor before use. 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. Do not use if safety seal is broken or missing.