Arnica Montana, Benzoic Acid, Bryonia Alba Root, Matricaria Recutita, Solanum Dulcamara Top, Potassium Iodide, Pulsatilla Vulgaris, Rhododendron Aureum Leaf, Toxicodendron Pubescens Leaf
FDA Drug Information • Also known as: Arnicare Arthritis
- Brand Names
- Arnicare Arthritis
- Drug Class
- Nitrogen Binding Agent [EPC]
- Route
- ORAL
- Dosage Form
- TABLET
- Product Type
- HUMAN OTC DRUG
What Is Arnica Montana, Benzoic Acid, Bryonia Alba Root, Matricaria Recutita, Solanum Dulcamara Top, Potassium Iodide, Pulsatilla Vulgaris, Rhododendron Aureum Leaf, Toxicodendron Pubescens Leaf Used For?
Uses* Temporary relieves minor aches and pains associated with arthritis
Dosage and Administration
Directions Adults 18 years of age and older: At the onset of symptoms, dissolve 2 tablets under the tongue and repeat, if needed, every 15 minutes for 3 more doses. Then, dissolve 2 tablets under the tongue every hour until symptoms improve. Children under 18 years of age: Ask a doctor.
About This Information
This drug information is sourced from FDA-approved labeling via the openFDA database. It is intended for educational and reference purposes only. This is not medical advice. Always consult your healthcare provider before making decisions about medication. Drug information may be updated by the FDA; check with your pharmacist for the most current information.
What are side effects?
Side effects are unwanted reactions that can occur when taking a medication. They range from mild (headache, nausea) to severe (allergic reactions, organ damage). Not everyone experiences side effects, and severity varies. Report any concerning side effects to your doctor.
What are drug interactions?
Drug interactions occur when a medication is affected by another drug, food, or supplement. Interactions can make medications less effective or cause dangerous side effects. Always tell your doctor about all medications and supplements you take.