Naximin (Spray) Instructions for Use
Marketing Authorization Holder
Grotex, LLC (Russia)
ATC Code
R01AB06 (Xylometazoline in combination with other drugs)
Active Substances
Dexpanthenol (Rec.INN registered by WHO)
Xylometazoline (Rec.INN registered by WHO)
Dosage Forms
| Naximin | Metered dose nasal spray 0.1 mg+5 mg/1 dose: 10 ml (90 doses) or 15 ml (135 doses) bottle | |
| Metered dose nasal spray 0.05 mg+5 mg/1 dose: 10 ml (90 doses) or 15 ml (135 doses) bottle |
Dosage Form, Packaging, and Composition
Metered dose nasal spray in the form of a transparent, colorless or slightly yellowish solution.
| 1 dose | |
| Xylometazoline hydrochloride | 0.1 mg |
| Dexpanthenol | 5 mg |
Excipients: potassium dihydrogen phosphate – 0.9 mg, disodium hydrogen phosphate dihydrate – 0.015 mg, purified water – up to 100 µl.
10 ml (90 doses) – polyethylene bottles (1) with a dosing nozzle – cardboard packs.
15 ml (135 doses) – polyethylene bottles (1) with a dosing nozzle – cardboard packs.
Metered dose nasal spray in the form of a transparent, colorless or slightly yellowish solution.
| 1 dose | |
| Xylometazoline hydrochloride | 0.05 mg |
| Dexpanthenol | 5 mg |
Excipients: potassium dihydrogen phosphate – 0.9 mg, disodium hydrogen phosphate dihydrate – 0.015 mg, purified water – up to 100 µl.
10 ml (90 doses) – polyethylene bottles (1) with a dosing nozzle – cardboard packs.
15 ml (135 doses) – polyethylene bottles (1) with a dosing nozzle – cardboard packs.
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, combinations without corticosteroids
Pharmacological Action
Combined medicinal product for topical application.
Xylometazoline belongs to the group of topical vasoconstrictors (decongestants) with alpha-adrenomimetic activity, causes constriction of the blood vessels of the nasal mucosa, restores the patency of the nasal passages, and facilitates nasal breathing. The drug’s effect usually begins a few minutes after application and lasts up to 10 hours.
Dexpanthenol is a B vitamin – a derivative of pantothenic acid. Dexpanthenol is converted in the body into pantothenic acid, which is a component of coenzyme A and is involved in acetylation processes, carbohydrate and fat metabolism, in the synthesis of acetylcholine, corticosteroids, porphyrins; it stimulates the regeneration of the skin and mucous membranes, normalizes cellular metabolism, accelerates mitosis and increases the strength of collagen fibers. It has a regenerating, metabolic and weak anti-inflammatory effect.
Pharmacokinetics
Xylometazoline is practically not absorbed when applied topically; plasma concentrations are so low that they cannot be determined by modern analytical methods.
Dexpanthenol is rapidly absorbed through the skin when applied topically and is converted into pantothenic acid, which binds to plasma proteins (mainly to beta-globulin and albumin). Its concentration in blood is 0.5-1 mg/l, in blood serum – 100 µg/l. Pantothenic acid is not metabolized in the body (except for inclusion in CoA) and is excreted unchanged.
Indications
Acute respiratory diseases with symptoms of rhinitis; acute allergic rhinitis; vasomotor rhinitis; sinusitis; otitis media (as part of combination therapy to reduce swelling of the nasopharyngeal mucosa); to facilitate rhinoscopy; to restore impaired nasal breathing after surgical interventions in the nasal cavity.
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 |
| J30.0 | Vasomotor rhinitis |
| 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 |
| CA08.3 | Vasomotor 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. |
For intranasal administration only. Use the 0.1 mg+5 mg/dose formulation for adults and children over 6 years. Use the 0.05 mg+5 mg/dose formulation for children aged 2 to 6 years; this formulation is contraindicated for children under 2 years.
Administer one dose into each nostril. The recommended frequency is three to four times per day. The maximum duration of continuous treatment is five days.
Before administration, clear the nasal passages. Prime the spray pump with several actuations before first use or if not used for several days. Insert the nozzle into the nostril, keeping the bottle upright. Close the other nostril with a finger. Actuate the pump while inhaling gently through the nose. Repeat the procedure for the other nostril.
Do not exceed the recommended dosage or duration of treatment to avoid rebound congestion (medication-induced rhinitis) and systemic effects. If symptoms persist beyond 5 days, discontinue use and consult a physician.
Adverse Reactions
With frequent and/or prolonged use: irritation and/or dryness of the nasopharyngeal mucosa, burning, tingling, sneezing, hypersecretion, allergic reactions, swelling of the nasal mucosa, vomiting, headache, dry rhinitis, palpitations, increased blood pressure, insomnia, visual impairment, depression (with long-term use of high doses).
Contraindications
Arterial hypertension; tachycardia; severe atherosclerosis; atrophic rhinitis; hyperthyroidism; porphyria; prostatic hyperplasia; glaucoma; surgical interventions on the meninges (in history); children under 2 years of age; children under 6 years of age (for dosage forms intended for older children and adults); simultaneous therapy with MAO inhibitors and tricyclic antidepressants; hypersensitivity to the components of the medicinal product.
With caution
Diabetes mellitus, pheochromocytoma.
Use in Pregnancy and Lactation
Use during pregnancy and lactation (breastfeeding) is not recommended.
Pediatric Use
Contraindicated in children under 6 years of age.
Special Precautions
Before use, it is necessary to clean the nasal passages.
Should not be used for more than 5 days.
Effect on ability to drive vehicles and mechanisms
During the period of use, precautions should be observed, or driving vehicles and engaging in other potentially hazardous activities that require increased concentration and speed of psychomotor reactions should be avoided.
Drug Interactions
With simultaneous use of MAO inhibitors and tricyclic antidepressants, an increase in systemic action is possible.
Storage Conditions
Store at 2°C (36°F) to 25°C (77°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 Disclaimer
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