Xylo (Spray) Instructions for Use
ATC Code
R01AA07 (Xylometazoline)
Active Substance
Xylometazoline (Rec.INN registered by WHO)
Clinical-Pharmacological Group
Vasoconstrictor drug for topical use in ENT practice
Pharmacotherapeutic Group
Drugs for the treatment of nasal diseases; decongestants and other drugs for topical use; sympathomimetics
Pharmacological Action
Vasoconstrictor for topical use in ENT practice. Alpha-adrenomimetic. When applied to the mucous membranes, it causes constriction of the blood vessels of the nasal mucosa, thereby eliminating swelling and hyperemia of the nasal mucosa, and restores the patency of the nasal passages. In rhinitis, it facilitates nasal breathing.
Pharmacokinetics
When applied topically, it is practically not absorbed; plasma concentrations are so low that they cannot be determined by modern analytical methods.
Indications
To reduce swelling of the nasopharyngeal mucosa and discharge in acute allergic rhinitis, acute respiratory infections with symptoms of rhinitis, sinusitis, hay fever, otitis media; preparation of the patient for diagnostic procedures in the nasal passages.
ICD codes
| ICD-10 code | Indication |
| H66 | Suppurative and unspecified otitis media |
| J00 | Acute nasopharyngitis (common cold) |
| J01 | Acute sinusitis |
| J06.9 | Acute upper respiratory infection, unspecified |
| J30.1 | Allergic rhinitis due to pollen |
| J30.3 | Other allergic rhinitis (perennial allergic rhinitis) |
| J32 | Chronic sinusitis |
| Z51.4 | Preparatory procedures for subsequent treatment or examination, not elsewhere classified |
| ICD-11 code | Indication |
| AA9Z | Unspecified suppurative otitis media |
| CA00 | Acute nasopharyngitis |
| CA01 | Acute rhinosinusitis |
| CA07.0 | Acute upper respiratory tract infection of unspecified site |
| CA08.00 | Allergic rhinitis due to pollen |
| CA08.03 | Other allergic rhinitis |
| CA0A.Z | Chronic rhinosinusitis, unspecified |
| QB9A | Preparatory procedures for subsequent treatment |
Dosage Regimen
| The method of application and dosage regimen for a specific drug depend on its form of release and other factors. The optimal dosage regimen is determined by the doctor. It is necessary to strictly adhere to the compliance of the dosage form of a specific drug with the indications for use and dosage regimen. |
Administer the spray intranasally only. The dose is strictly dependent on the patient’s age and the specific product concentration.
For adults and children aged 12 years and older: administer one spray into each nostril. Use up to three times per day as needed for nasal congestion.
For children aged 6 to 11 years: use only the pediatric formulation (0.05% concentration). Administer one spray into each nostril. The interval between applications should not be less than 8-10 hours. Do not exceed two administrations in a 24-hour period.
Do not use this product in children under 6 years of age unless explicitly directed by a physician. The risk of systemic adverse effects is higher in this age group.
Clear the nasal passages before use. Keep the head upright; do not tilt it backward. Insert the tip of the spray bottle into the nostril. Press down firmly and quickly to release the spray while breathing in gently through the nose. Repeat the procedure for the other nostril.
The maximum duration of continuous use is 7 days. Do not exceed the recommended dosage or frequency of administration. Prolonged use can lead to rebound congestion (medication-induced rhinitis) and atrophy of the nasal mucosa.
If symptoms persist beyond 7 days, discontinue use and consult a physician for further evaluation. To avoid contamination, do not share the bottle with another person.
Adverse Reactions
From the immune system – uncommon: hypersensitivity reactions (angioedema, skin rash, itching).
From the digestive system – rare: nausea, vomiting.
From the nervous system – rare: headache; very rare: insomnia, anxiety, fatigue, hallucinations, and convulsions (mainly in children).
From the organ of vision – very rare: blurred vision.
From the cardiovascular system – rare: palpitations, increased blood pressure, tachycardia; very rare: arrhythmia.
Local reactions – common: irritation and/or dryness of the nasopharyngeal mucosa, burning and paresthesia of the nasal mucosa, sneezing, hypersecretion of the nasal mucosa; uncommon: swelling of the nasal mucosa, nosebleeds, withdrawal syndrome. Increased swelling of the nasal mucosa (reactive hyperemia) is possible.
Contraindications
Hypersensitivity to xylometazoline; atrophic rhinitis, thyrotoxicosis; inflammatory diseases of the skin or mucous membrane of the nasal vestibule; condition after transsphenoidal hypophysectomy; patients with severe cardiovascular diseases (e.g., coronary artery disease, angina pectoris, tachycardia, arterial hypertension, severe atherosclerosis); patients with a history of surgical interventions on the meninges; patients taking MAO inhibitors or other drugs that can cause increased blood pressure; patients with increased intraocular pressure, especially with angle-closure glaucoma; during therapy with tricyclic and tetracyclic antidepressants, other topical vasoconstrictors (decongestants); pregnancy; pediatric age – depending on the dosage form.
With caution in patients with hypersensitivity to adrenomimetics, accompanied by symptoms of insomnia, dizziness, arrhythmia, tremor, increased blood pressure; patients with pheochromocytoma, porphyria; patients with endocrine diseases (e.g., hyperthyroidism, diabetes mellitus); patients with prostatic hyperplasia; during lactation (breastfeeding).
Use in Pregnancy and Lactation
Contraindicated for use during pregnancy. During lactation, use is possible only as prescribed by a doctor, after a thorough assessment of the benefit-risk ratio for the mother and the potential risk to the child. Exceeding the recommended doses is not allowed.
Pediatric Use
Use in children is possible according to indications, in age-appropriate recommended doses and dosage forms. It is necessary to strictly follow the instructions in the drug labels for xylometazoline regarding contraindications for use in children of different ages for specific dosage forms of xylometazoline. The recommended doses should not be exceeded in children.
Geriatric Use
The recommended doses should not be exceeded in elderly patients.
Special Precautions
Long-term use (more than 7 days) and overdose of sympathomimetics with a decongestant effect can lead to reactive hyperemia of the nasal mucosa. As a result, nasal breathing difficulty occurs, which leads to the patient starting to use xylometazoline repeatedly or even constantly. This can lead to chronic swelling (medication-induced rhinitis), and ultimately even to atrophy of the nasal mucosa (ozena).
In milder cases, to improve the patient’s condition, it is possible to initially stop the administration of the sympathomimetic in one nostril, and after the complaints decrease, continue to administer it into the other nostril to at least partially ensure nasal breathing.
The recommended doses should not be exceeded, especially in children and elderly patients.
Effect on the ability to drive vehicles and operate machinery
With long-term treatment or when using xylometazoline in higher doses, the possibility of its systemic action cannot be excluded. In case of systemic side effects, it is necessary to refrain from driving vehicles and engaging in other potentially hazardous activities that require increased concentration and speed of psychomotor reactions.
Drug Interactions
Enhancement of the systemic action of xylometazoline is possible with simultaneous use of MAO inhibitors and tricyclic antidepressants. Simultaneous use of xylometazoline with tetracyclic antidepressants, other topical vasoconstrictors (decongestants), as well as other drugs that increase blood pressure is incompatible.
Storage Conditions
Store at 2°C (36°F) to 30°C (86°F). Keep in original packaging, protected from light. Keep out of reach of children.
Dispensing Status
Over-the-Counter
Important Safety Information
This information is for educational purposes only and does not replace professional medical advice. Always consult your doctor before use. Dosage and side effects may vary. Use only as prescribed.
Medical DisclaimerBrand (or Active Substance), Marketing Authorisation Holder, Dosage Form
Metered nasal spray 140 mcg/dose
Marketing Authorization Holder
Severnaya Zvezda NAO (Russia)
Dosage Form
| Xylo Nordum® | Metered nasal spray 140 mcg/dose |
Dosage Form, Packaging, and Composition
Metered nasal spray
| 1 dose | |
| Xylometazoline hydrochloride | 140 mcg |
15 ml – bottles – carton packs – Over-the-Counter
20 ml – bottles – carton packs – Over-the-Counter
Nasal spray, metered 0.1 mg/dose: vial 10 ml or 15 ml
Marketing Authorization Holder
Pharmtekhnologiya LLC (Republic of Belarus)
Dosage Form
| Xylo with menthol and eucalyptus | Nasal spray, metered 0.1 mg/dose: vial 10 ml or 15 ml |
Dosage Form, Packaging, and Composition
Metered nasal spray in the form of a colorless or almost colorless, transparent or slightly opalescent solution with a characteristic smell of menthol and eucalyptus.
| 1 dose (0.1 ml) | |
| Xylometazoline hydrochloride | 0.1 mg |
Excipients: sodium dihydrogen phosphate dihydrate, disodium phosphate dodecahydrate, sodium chloride, benzalkonium chloride, non-crystallizing sorbitol solution, disodium edetate, levomenthol, eucalyptol (cineole), macrogolglycerol hydroxystearate, purified water.
10 ml (80 doses) – bottles (1) with spray nozzles – carton packs.
15 ml (100 doses) – bottles (1) with spray nozzles – carton packs.
Nasal spray, metered 140 mcg/1 dose: vial 15 ml or 20 ml
Marketing Authorization Holder
Severnaya Zvezda NAO (Russia)
Dosage Form
| Xylo Nordum® with menthol and eucalyptus | Nasal spray, metered 140 mcg/1 dose: vial 15 ml or 20 ml |
Dosage Form, Packaging, and Composition
Metered nasal spray
| Xylometazoline | 140 mcg/dose |
15 ml – bottles – carton packs – Over-the-Counter
20 ml – bottles – carton packs – Over-the-Counter
