MUNDIPUR
MUNDIPUR is an FDA drug label for the active ingredient BRYONIA DIOICA ROOT, COLCHICUM AUTUMNALE BULB, SODIUM CARBONATE, PHYTOLACCA AMERICANA ROOT, BERBERIS VULGARIS ROOT BARK, CYNARA SCOLYMUS WHOLE, HARPAGOPHYTUM PROCUMBENS ROOT, AND LEDUM PALUSTRE TWIG manufactured by PEKANA Naturheilmittel GmbH administered by ORAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20221216.
- Generic name
- BRYONIA DIOICA ROOT, COLCHICUM AUTUMNALE BULB, SODIUM CARBONATE, PHYTOLACCA AMERICANA ROOT, BERBERIS VULGARIS ROOT BARK, CYNARA SCOLYMUS WHOLE, HARPAGOPHYTUM PROCUMBENS ROOT, AND LEDUM PALUSTRE TWIG
- Manufacturer
- PEKANA Naturheilmittel GmbH
- Product type
- HUMAN OTC DRUG
- Route
- ORAL
- Dosage form
- N/A
- NDC
- 59469-140
- Application
- N/A
- Label effective
- 20221216
Active ingredients
Indications & Usage
Indications For relief of occasional minor rheumatic symptoms such as stiffness and joint pain. Application of this homeopathic remedy for the designated usage is exclusively based on homeopathic experience. With severe forms of this disease, a clinically proven therapy is indicated.
Dosage & Administration
Dosage Unless otherwise prescribed, adults take 15-20 drops, 3 times per day. For pediatric dosages, consult your practitioner.
Contraindications
Not available.
Warnings
Warning If symptoms persist, contact a licensed practitioner. If you have known sensitivity to any of the ingredients, please consult your licensed practitioner before use. If you are pregnant or nursing a baby, seek the advice of a health care professional before use. Keep out of the reach of children. Protect from light and heat. Tamper Evident Do not use this product if tamper evident strip is broken or removed from base of cap.
Adverse Reactions
Not available.