Patient information leaflet
Read leaflet before use. The leaflet describes indications, contraindications, and gives information about adverse reactions and dosage, as well as about administration of the medicinal product. Otherwise consult a doctor or a pharmacist as improper use of any pharmaceutical product can pose a danger to life and health.
Active substance
composite preparation; 100 g of gel contain the following active ingredients: dry extract of (6-12:1) Matricaria chamomilla flower 2.0 parts, Calendula officinalis 0.5 part, Tussilago farfara leaf 1.4 parts, Quercus cortex 3.0 parts, Salvia officinalis leaf 2.0 parts, Thymus vulgaris herb 1.0 parts (extractants: methanol 90% [v/v], water) – 10.0g; allantoin 0.1 g; camomile essential oil 0.3 g; peppermint essential oil 0.3 g.
Indications
Superficial application for styptic, anti-inflammatory and antibacterial effect with topical anaesthetic action, and accelerated growth of granulation tissue and healing of wounds. The pharmaceutical product is intended for topical administration on oral cavity mucosa helping in the treatment of periodontal disease and inflammation of the oral cavity (e.g. decubitus ulcers from dental prosthetics). The product can be administered in post periodontal surgery only as recommended by the dental surgeon.
Dosage and administration
Adults and adolescents over 12 years of age: administer Mucosit® directly after brushing teeth by rubbing a 1-2 cm strip into the gums 2 to 3 times a day for 3 minutes with a finger tip or a soft brush. If applying with fingers, wash the hands thoroughly before and after application. The gel can also be applied with cosmetic swabs.
Contraindications
Hypersensitivity to topical anaesthetics or other ingredients of the drug. Persons allergic to birch pollen or celery may exhibit cross hypersentivity to thyme. Do not administer in hypersensitivity to Asteraceae plants, e.g. camomile, or Lamiaceae.
Responsible entity
Poznańskie Zakłady Zielarskie Herbapol S.A. in Poznań
