Zellulisan
Zellulisan is an FDA drug label for the active ingredient HORSE CHESTNUT, ARNICA MONTANA, BETULA PENDULA LEAF, HEDERA HELIX FLOWERING TWIG, LEDUM PALUSTRE TWIG, MELILOTUS OFFICINALIS TOP, TOXICODENDRON PUBESCENS LEAF, AND SULFUR manufactured by Pekana-Naturheilmittel GmbH administered by TOPICAL. 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 20221221.
- Generic name
- HORSE CHESTNUT, ARNICA MONTANA, BETULA PENDULA LEAF, HEDERA HELIX FLOWERING TWIG, LEDUM PALUSTRE TWIG, MELILOTUS OFFICINALIS TOP, TOXICODENDRON PUBESCENS LEAF, AND SULFUR
- Manufacturer
- Pekana-Naturheilmittel GmbH
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 59469-038
- Application
- N/A
- Label effective
- 20221221
Active ingredients
Indications & Usage
Uses Application of this homeopathic remedy for the designated usage is exclusively based on homeopathic experience. These "Uses" have not been evaluated by the Food and Drug Administration. With severe forms of this disease, a clinically proven therapy is indicated. For relief of minor tendinitis and inflammation
Dosage & Administration
Directions Unless otherwise prescribed, apply a moderate amount of ointment 2 to 3 times per day by rubbing gently into the affected area.
Contraindications
Not available.
Warnings
Warnings For external use only. Do not use on open wounds! 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.
Adverse Reactions
Not available.