Parapharmacy
Update of 17/06/2025
CE NÉCYRANE DM nasal spray
cold rhinopharyngitis allergic rhinitis
Forms and presentations
Solution for nasal instillation: Spray bottle of 10 ml (EAN 3573994005636).Composition
Water, sodium chloride, sodium levulinate, sodium phosphate, potassium sorbate, polyglyceryl-4 laurate/succinate, essential oil ofEucalyptus globulus, essential oil of Mentha piperita, disodium phosphate.Without propellant gas.
PROPERTIES and USE
The hypertonic nasal spray Nécyrane DM is a medical device intended to relieve the symptoms of colds, rhinopharyngitis and allergic rhinitis, in adults and children from 12 years of age.- Decongests, eases breathing and improves comfort.
- Reduces the duration of the cold.
- Forms a protective layer on the nasal mucosa that acts as a barrier against viruses and bacteria.
- Soothes and moisturises the irritated nasal mucosa.
- Sensation of coolness for immediate relief thanks to the presence of eucalyptus essential oil.
Directions for use
- Shake the bottle and blow your nose before use.
- Remove the protective cap.
- Hold the bottle upright and insert the spray nozzle into the nose.
- Spray 1 to 2 times into each nostril up to 6 times a day, for 3-7 days.
- Do not use for more than 30 days without interruption.
Precautions for use
Do not use in children under 12 years of age.
It is important for users to check the list of ingredients to ensure that the spray does not contain ingredients to which they are allergic.
In case of allergic reactions, stop using the product.
Contains eucalyptus essential oil: to be avoided by people with epilepsy.
Read the instructions in the leaflet carefully before use.
Keep out of reach of young children.
- Possible undesirable effects:
- Some people may feel nasal irritation and burning, and in very rare cases, nosebleeds may occur.
Fertility, pregnancy and breastfeeding
Do not use in pregnant or breastfeeding women in the absence of sufficient human data on the ingredients of Nécyrane DM.
STORAGE CONDITIONS
Store at room temperature (5-25 °C) in a dry, dark place, in its original container.ADMINISTRATIVE INFORMATION
| Class I medical device. | |
| Manufacturer: Peters Krizman AG, Switzerland. | |
| Authorised representative in the European Union: PK Benelux BV, Belgium. | |
| Distributor: Pierre Fabre Médicament, France. |
PIERRE FABRE MEDICAMENT
Les Cauquillous. 81500 Lavaur
Medical info:
Materiovigilance: Tel: 01 49 10 96 18
Source: VIDAL · Updated on 11/11/2026. This information does not replace advice from a healthcare professional.