


Ask a doctor about a prescription for AMNIOLINA POMADA OINTMENT
Leaflet: information for the user
AMNIOLINA ointment
Zinc oxide/ Talc
Read the entire leaflet carefully before starting to use this medication, as it contains important information for you.
Follow the administration instructions of the medication contained in this leaflet or as indicated by your doctor or pharmacist.
Contents of the leaflet
It contains zinc oxide and talc as active ingredients. Zinc oxide is a skin protector that acts as a barrier between the skin and irritants, and talc relieves skin irritations; they facilitate healing.
Amniolina is indicated for the prevention and treatment of diaper area dermatitis (inflammation and irritation of the skin in contact with the diaper) and for the prevention of chafing and irritations in other areas of friction with clothing or other areas of the skin.
Amniolina ointment is indicated for children and incontinent adults.
Do not use Amniolina
Warnings and precautions
Consult your doctor or pharmacist before starting to use Amniolina ointment.
Children
This medication is indicated for children. The usual precautions are required in babies and children.
Using Amniolina ointment with other medications
Tell your doctor or pharmacist if you are using, have recently used, or may need to use any other medication.
Pregnancy and breastfeeding
If you are pregnant or breastfeeding, think you may be pregnant, or plan to become pregnant, consult your doctor or pharmacist before using this medication.
In necessary cases, you can use this medication if necessary, with due precautions.
Driving and using machines:
This medication does not affect the ability to drive and use machines.
Amniolina ointment contains lanolin
This medication may cause local skin reactions (such as contact dermatitis) because it contains lanolin.
Follow the administration instructions of the medication contained in this leaflet or as indicated by your doctor or pharmacist. In case of doubt, ask your doctor or pharmacist.
For external use (on the skin).
Apply the ointment regularly to the area to be treated, usually after a diaper change.
Method of use
Clean and dry the area to be protected or treated well. Apply Amniolina to the area, spreading the ointment with your fingertips in a smooth but insistent manner, until you cover the entire surface of the skin to be protected or treated with a thin layer, without forgetting the folds and creases of the affected area.
The application of Amniolina should always be done after bathing and as many other times as necessary, usually coinciding with diaper changes: insisting particularly on those parts most prone to injury (diaper friction, prolonged contact with feces, etc.).
If you use more Amniolina than you should
No possibility of intoxication is expected if the product is used as recommended.
Prolonged use of this medication may cause irritation.
In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately or call the Toxicology Information Service, phone 91 562 04 20, indicating the medication and the amount ingested.
If you forget to use Amniolina
Do not use a double dose to make up for forgotten doses.
Apply Amniolina when it is due.
If you stop treatment with Amniolina
If you have any other doubts about using this medication, ask your doctor or pharmacist.
Like all medications, this medication can cause side effects, although not everyone experiences them.
In rare cases, hypersensitivity to one of its components may occur (local or general allergic manifestations in sensitive individuals (rash, irritation, etc.).
Reporting 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 Medication Surveillance System for Human Use: www.notificaRAM.es
By reporting side effects, you can contribute to providing more information on the safety of this medication.
No special storage conditions are required.
Keep this medication out of the sight and reach of children.
Do not use this medication after the expiration date shown on the packaging after CAD. The expiration date is the last day of the month indicated.
Medications should not be thrown away in drains or trash. Deposit the packaging and medications you no longer need at the SIGRE point in the pharmacy. If in doubt, ask your pharmacist how to dispose of the packaging and medications you no longer need. This way, you will help protect the environment.
Composition of AMNIOLINA ointment
Appearance of the product and package contents
This medication is presented in the form of an ointment, which is white, greasy to the touch, and has a rose scent.
Each box contains a tube with 50 g of ointment.
Marketing authorization holder
LABORATORIO REIG JOFRE, S.A.
Avda. Gran Capitan, 10
08970 Sant Joan Despí (Barcelona)
Manufacturer
BIOGLAN AB
Borrgatan 31,
211 24, Malmö
Sweden
Date of the last revision of this leaflet:04/2021.
Detailed information about this medication 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 AMNIOLINA POMADA OINTMENT – subject to medical assessment and local rules.