Methylrosanilinium chloride
1 g of solution contains
active substance:methylrosanilinium chloride 5 mg,
excipients:purified water.
20 g
EAN Code: 5909990668212
100 g
EAN Code: 5909990668229
Application to the skin.
Store the medicine in a place invisible and inaccessible to children.
Do not use after the expiry date.
Store at a temperature below 25°C, in the original packaging.
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PPF HASCO-LEK S.A.
51-131 Wrocław, ul. Żmigrodzka 242 E
(Logo of the marketing authorisation holder)
OTC - Medicine available without a prescription.
For the treatment of superficial skin and mucous membrane damage, and for use in purulent skin and mucous membrane infections, some fungal and yeast infections.
Do not use in case of hypersensitivity to methylrosanilinium chloride. Do not use in patients with porphyria.
Do not use in the eyes, on granulating or ulcerating lesions on the face. Methylrosanilinium chloride stains tissues, stains fabrics and clothing. Stains on fabrics can be removed with a mixture of ethanol and acetic acid.
Acidification or colloidal hydrated aluminium silicate (bentonite) weakens the effect of the medicine.
If the patient is pregnant or breastfeeding, or thinks she may be pregnant or plans to have a child, she should consult a doctor or pharmacist before using this medicine.
The medicine has no effect or a negligible effect on the ability to drive and use machines.
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The medicine should be used externally - locally, as a disinfectant.
In case of doubt, consult a doctor or pharmacist.
In case of accidental ingestion of the medicine, consult a doctor.
Prolonged and frequent use, especially in children, may cause irritation or ulceration of the skin or mucous membranes in direct contact with the medicine. After application of methylrosanilinium chloride in children in cases of oral mucous membrane thrush, cases of respiratory distress associated with severe irritation of the upper respiratory tract mucous membranes have been reported.
If any undesirable effects occur, including any undesirable effects not listed on the label, consult a doctor or pharmacist. Undesirable effects can be reported directly to the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products: e-mail: ndl@urpl.gov.pl, tel.: (22) 49 21 301. Undesirable effects can also be reported to the marketing authorisation holder.
gencjana 0.5% aqueous solution
Not applicable.
Not applicable.
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