


Ask a doctor about a prescription for BLASTOESTIMULINA 10 mg/g OINTMENT
Leaflet: information for the user
Blastoestimulina 10 mg/g ointment
extract of Centella asiatica
Read this leaflet carefully before starting to use this medicine, as it contains important information for you.
Follow the instructions for administration of the medicine contained in this leaflet or as indicated by your doctor, pharmacist, or nurse.
Contents of the leaflet
Blastoestimulina contains as an active ingredient extract of Centella asiatica, with wound-healing action.
Blastoestimulina is indicated for wound healing, fissures, ulcers, sores, bedsores, and other skin erosions (or cracks). It is also indicated for the healing of minor burns and post-operative wounds.
Do not useBlastoestimulina
Warnings and precautions
Consult your doctor, pharmacist, or nurse before starting to use Blastoestimulina.
Do not ingest. For external use only (on the skin).
Do not use this medicine for extended periods or on infected wounds.
If you do not observe clinical improvement after 7 days of treatment, you should consult your doctor, who will review the suitability of the treatment.
Children and adolescents
This medicine is not recommended for children and adolescents due to the lack of safety and efficacy data in this population.
Other medicines and Blastoestimulina
Inform your doctor or pharmacist if you are using, have recently used, or may need to use any other medicine.
To date, no interactions are known.
Pregnancy, breastfeeding, and fertility
If you are pregnant or breastfeeding, think you may be pregnant, or plan to become pregnant, consult your doctor or pharmacist before using this medicine.
There are no data on the use of this medicine during pregnancy or breastfeeding, so the use of Blastoestimulina is not recommended during pregnancy and breastfeeding.
Driving and using machines
The use of Blastoestimulina does not produce adverse effects on the ability to drive or use machines.
Blastoestimulina contains propylene glycol (E-1520), diethylene glycol palmitostearate, and fragrances that contain allergens
This medicine contains 291 mg of propylene glycol and 171 mg of diethylene glycol palmitostearate per gram of ointment.
Propylene glycol and diethylene glycol palmitostearate may cause skin irritation. Do not use on open wounds or large areas of damaged skin (such as burns) without consulting your doctor or pharmacist first.
This medicine contains fragrances with allergens, such as geranium essence with: citronellol, geraniol, linalool, citral, and d-limonene; and lavender essence with: linalool, d-limonene, coumarin, geraniol, citronellol, benzyl alcohol, benzyl cinnamate, anisic alcohol, amylcinnamaldehyde, 3-methyl-4-(2,6,6-trimethyl-2-cyclohexen-1-yl)-3-buten-2-one, and citral.
Allergens may cause allergic reactions.
Follow the instructions for administration of the medicine contained in this leaflet or as indicated by your doctor, pharmacist, or nurse. In case of doubt, ask your doctor or pharmacist.
For external use only. Do not ingest.
The recommended dose in adults is: apply the ointment 1 to 3 times a day, in sufficient quantity to obtain a thin layer on the area to be treated. It is recommended to clean the affected area before starting treatment, removing any organic residue.
If you use more Blastoestimulina than you should
Due to its external use, it is unlikely that cases of intoxication will occur, unless it is accidentally used on large areas of skin and at doses much higher than recommended.
In case of overdose or accidental ingestion, consult the Toxicology Information Service, phone 915 620 420, or consult your doctor or pharmacist.
If you have any other questions about the use of this medicine, ask your doctor, pharmacist, or nurse.
Like all medicines, this medicine can cause side effects, although not everyone gets them.
Application of this product may cause itching, burning, skin irritation, and contact dermatitis (red rash on the skin, with itching, due to contact with a substance).
Reporting of side effects
If you experience any type of side effect, consult your doctor or pharmacist, even if it is a possible side effect not listed in this leaflet. You can also report them directly through the Spanish Pharmacovigilance System for Human Use Medicines: https://www.notificaram.es. By reporting side effects, you can contribute to providing more information on the safety of this medicine.
Keep this medicine out of the sight and reach of children.
Store below 30°C.
Do not use this medicine after the expiration date that appears on the packaging after CAD. The expiration date is the last day of the month indicated. Once the packaging is opened, discard after 3 months.
Medicines should not be thrown away through wastewater or household waste. Deposit the packaging and medicines you no longer need at the SIGRE point in the pharmacy. Ask your pharmacist how to dispose of the packaging and medicines you no longer need. This will help protect the environment.
Composition of Blastoestimulina 10 mg/g ointment
Appearance of the product and package contents
Blastoestimulina is a white to creamy white ointment.
It is presented in polyethylene tubes of 30g or 60g of ointment.
Marketing authorization holder and manufacturer
Marketing authorization holder
Almirall, S.A.
General Mitre, 151
08022 Barcelona (Spain)
Manufacturer
Industrias Farmacéuticas Almirall, S.A.
Ctra. de Martorell, 41-61
08740 Sant Andreu de la Barca – Barcelona (Spain)
Almirall Hermal GmbH
Scholtzstrasse 3
21465 Reinbek
Germany
Date of the last revision of this leaflet:December 2021.
Detailed information about this medicine is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) (http://www.aemps.gob.es)
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Discuss dosage, side effects, interactions, contraindications, and prescription renewal for BLASTOESTIMULINA 10 mg/g OINTMENT – subject to medical assessment and local rules.