Descrizione Clinica
First aid Fylladerm cream ac ialur 32g Fylladerm
FYLLAderm
Cream based on Hyaluronic Acid and Natural Extracts
Description
Medical device Class IIB (Directive 93/42/EEC). Not sterile.
Non-invasive device used for topical treatment of dermo-epidermal tissue alterations, requiring reactivation of epithelial neoformation processes. Thanks to its formulation:
- accelerates physiological processes of tissue repair;
- protects the injury from microbial contamination;
- keeps the environment of injury humid;
- promotes the free drainage of the exudate.
Product free from latex.
Mode of use
Before applying the area concerned. Apply directly on the lesion forming a uniform layer. If necessary, cover with a sterile gauze and fix with bandage or with bandage. The number of applications depends on the clinical condition of the skin injury and varies depending on the clinical protocol indicated by the doctor.
Components
PEG 400, PEG 1500, PEG 4000, Sorbitol, Glicerol, Water, Menthol, Allantoin, Vasellina, Sodium Hyaluronate E.S. Centella Asiatica, E.S. Dioic urtica, Cetilic Alcohol, Stearilic Alcohol, Phenoxyethanol, Etylglycerin, Acetate Tocopherol, O. E. Malaleuca Alternifolia.
Warnings
Do not use in sensitive cases known to product components. Prolonged use may lead to awareness-raising. In this case it is recommended to stop the therapy immediately and consult the doctor. Keep the device out of reach of children. Do not use if the packaging is not integrated. Do not use beyond the expiry date indicated on the package. Don't swallow. Carefully close the pipe after use. Do not apply the end of the tube on the wound.
In case of home use, the device can be disposed of as assimilable refusal to undifferentiated urban spaces. In the hospital environment it must be disposed of as a clinical refusal according to the current legislation.
Conservation
Store in a cool and dry place, sheltered from heat, light and humidity.
Validity of packaging: 36 months.
Format
32 g pipe.
Cod. 3
Medical device Class IIB (Directive 93/42/EEC). Not sterile.
Non-invasive device used for topical treatment of dermo-epidermal tissue alterations, requiring reactivation of epithelial neoformation processes. Thanks to its formulation:
- accelerates physiological processes of tissue repair;
- protects the injury from microbial contamination;
- keeps the environment of injury humid;
- promotes the free drainage of the exudate.
Product free from latex.
Mode of use
Before applying the area concerned. Apply directly on the lesion forming a uniform layer. If necessary, cover with a sterile gauze and fix with bandage or with bandage. The number of applications depends on the clinical condition of the skin injury and varies depending on the clinical protocol indicated by the doctor.
Components
PEG 400, PEG 1500, PEG 4000, Sorbitol, Glicerol, Water, Menthol, Allantoin, Vasellina, Sodium Hyaluronate E.S. Centella Asiatica, E.S. Dioic urtica, Cetilic Alcohol, Stearilic Alcohol, Phenoxyethanol, Etylglycerin, Acetate Tocopherol, O. E. Malaleuca Alternifolia.
Warnings
Do not use in sensitive cases known to product components. Prolonged use may lead to awareness-raising. In this case it is recommended to stop the therapy immediately and consult the doctor. Keep the device out of reach of children. Do not use if the packaging is not integrated. Do not use beyond the expiry date indicated on the package. Don't swallow. Carefully close the pipe after use. Do not apply the end of the tube on the wound.
In case of home use, the device can be disposed of as assimilable refusal to undifferentiated urban spaces. In the hospital environment it must be disposed of as a clinical refusal according to the current legislation.
Conservation
Store in a cool and dry place, sheltered from heat, light and humidity.
Validity of packaging: 36 months.
Format
32 g pipe.
Cod. 3
