Dr. Michaels Soratinex Gel 200 ml
What you should know about the medical device SORATINEX DR. MICHAEL'S GEL 200ML
This leaflet informs the user about the benefits and possible risks when using the medical device SORATINEX DR. MICHAEL'S GEL 200ML. Keep this leaflet together with the package of SORATINEX DR. MICHAELS GEL 200ML for viewing later. Always read the information for use carefully and note all warnings. Use SORATINEX DR. MICHAELS GEL 200ML only until the expiration of the indicated period of use or expiration date. Never dilute the product or mix it with other products. Always apply the Gel only with clean hands or an applicator that is carefully washed regularly with soap or a mild detergent. If you use applicators to apply the Gel, make sure that they are always washed after use and always let them dry completely before the next use. Do not share the product with anyone else.
What is the Soratinex Dr. medical device for? Does Michaels Gel 200ml use?
SORATINEX DR. MICHAELS GEL 200ML is used for the care of dry, flaky and inflamed skin on the scalp and body in adults, to relieve scaling caused by psoriasis. For best results it is recommended to use SORATINEX DR. MICHAELS GEL 200ML in combination with medical device SORATINEX DR. MICHAELS CREAM 250g or 50g and SORATINEX DR. MICHAELS OIL 200ml because they complement each other.
This product is only effective as part of a set.
Use of a medical device
SORATINEX DR. Use MICHAELS GEL 200ml once a day before applying SORATINEX DR. MICHAELS CREAM 250g or 50g and then treat the affected area with SORATINEX DR. MICHAELS OIL 200ml. SORATINEX DR. Apply MICHAELS GEL 200ml to wet skin, lather with a sponge or applicator and rinse with warm water after 2-3 minutes.
Before you start using the medical device
Before you start using the medical device SORATINEX DR. MICHAELS GEL 200ml ALWAYS test a small amount of the gel on a small area of the skin before use, as a test for possible reactions, especially if you are going to use the gel on sensitive areas of the skin. Leave on the skin for 24-48 hours, then wash off. If any reaction occurs, please contact the manufacturer immediately. If you have no reaction, apply SORATINEX DR. MICHAELS GEL 200ML according to the instructions for use.
Follow the recommended frequency of use
If you will use the medical device SORATINEX DR. MICHAELS GEL 200ML less often than you should, it is possible that it will not have as good effects and problems with dry, flaky and inflamed skin may persist. If you will use SORATINEX DR. MICHAELS GEL 200ML more often than you should, problems with dry, flaky and/or inflamed skin will not stop faster, on the contrary, you can irritate the skin even more.
Not intended for children under 3 years of age. Contains salicylic acid. Do not bring the product close to the eyes. Do not use on injured or inflamed skin. Wash the skin thoroughly after using the product. If you experience skin irritation, see a doctor. Before exposing your skin to the sun, apply a cream with a protective factor to the areas where you have applied the gel. Contains AHA (glycolic acid, citric acid). Folliculitis may occur in less than 1% of patients.
Safety and storage
Keep out of reach of children. In case of ingestion of the product, seek the emergency medical service of the nearest hospital. DO NOT induce vomiting. Close the cap carefully after each use. Do not store in direct sunlight or near heat sources. Store at a temperature of up to 25 C, but do not freeze.
The appearance of the medical device
SORATINEX DR. MICHAELS GEL 200ML is a thick liquid, transparent to opaque in color, with a characteristic smell.
alcohol, sodium laureth sulfate, cocamidopropyl betaine, triethanolamine, TEA laureth sulfate, salicylic acid, carbomer, glycolic acid, cocamide DEA, citric acid, tetrasodium EDTA, preservative Plantaserv/Geogard, purified water
Licensed to Tirsel Pty. Ltd., 374 Nepean Hwy , Frankston, VIC 3199, Australia Made in the EU for FRANKL Pharma sro, Štefánikova 248/32, 150 00 Prague 5, Czech Republic by Biotika Bohemia sro, Durychova 101, 142 00 Prague 4 Czech Republic,
Medical device of risk class 1 Manufacturer's certificate number: ISO 13485:2016 200330/A/0001/UK issued by URS - UNITED REGISTRAR OF SYSTEMS, UKAS member authorization number 0043, IAF member, www.urs-czech.cz