BRONCHI-PERTU
BRONCHI-PERTU is an FDA drug label for the active ingredient BRYONIA DIOICA ROOT, PROTORTONIA CACTI, GUAIACUM OFFICINALE RESIN, OENANTHE AQUATICA FRUIT, PHOSPHORUS, ANTIMONY POTASSIUM TARTRATE, USNEA BARBATA, AND GRINDELIA HIRSUTULA WHOLE 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 20221223.
- Generic name
- BRYONIA DIOICA ROOT, PROTORTONIA CACTI, GUAIACUM OFFICINALE RESIN, OENANTHE AQUATICA FRUIT, PHOSPHORUS, ANTIMONY POTASSIUM TARTRATE, USNEA BARBATA, AND GRINDELIA HIRSUTULA WHOLE
- Manufacturer
- PEKANA Naturheilmittel GmbH
- Product type
- HUMAN OTC DRUG
- Route
- ORAL
- Dosage form
- N/A
- NDC
- 59469-303
- Application
- N/A
- Label effective
- 20221223
Active ingredients
Indications & Usage
Indications Antitussive expextorant. 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 1 teaspoon up to 6 times per day, measured in a calibrated dosing cup. 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.