Product image of Nasoryl M (Xylometazoline Hydrochloride, Ipratropium Bromide) supplied by GNH India

Nasoryl M

Active Ingredient:
Xylometazoline Hydrochloride, Ipratropium Bromide
Origin:
EU

Nasoryl M (Xylometazoline Hydrochloride, Ipratropium Bromide)

Xylometazoline Hydrochloride and Ipratropium Bromide, the active ingredients in Nasoryl M, are a nasal decongestant and an anticholinergic agent presented as a nasal spray for intranasal use. They act together to relieve nasal congestion and reduce secretions in patients with rhinitis.
GNH India supplies Nasoryl M as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Jadran-Galenski Laboratorij D.D.

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Indications & Clinical Uses

Nasoryl M combines a decongestant and an anticholinergic to address conditions within the rhinitis spectrum.

  • Nasal congestion: reduces swelling of nasal mucosa to improve airflow.
  • Allergic rhinitis: limits reflex nasal secretions and eases blockage caused by allergens.
  • Non‑allergic rhinitis: diminishes mucosal edema and excessive discharge, supporting clearer breathing.

How It Works

  • Xylometazoline Hydrochloride acts as an alpha‑adrenergic agonist, causing vasoconstriction of the nasal submucosal vessels and thereby decreasing mucosal edema. Ipratropium Bromide blocks muscarinic receptors on nasal glands, inhibiting acetylcholine‑mediated secretions and reducing rhinorrhoea. The combined actions provide rapid decongestion and secretory control within the nasal passages.

Side Effects

Nasoryl M may cause a range of adverse reactions, most of which are mild and transient.

Common Side Effects

  • Nasal irritation or burning sensation.
  • Dryness of the nasal mucosa.
  • Sneezing or mild epistaxis.
  • Bitter taste after administration.
  • Headache.

Serious or Rare Side Effects

  • Severe allergic reaction (anaphylaxis) with swelling, rash, or difficulty breathing.
  • Persistent hypertension or tachycardia.
  • Nasal ulceration or perforation with prolonged use.
  • Acute angle‑closure glaucoma exacerbation.
  • Cardiac arrhythmias in susceptible individuals.

Precautions & Warnings

Before using Nasoryl M, consider the following safety measures.

  • Pregnancy: consult a healthcare professional before use.
  • Breastfeeding: discuss potential risks with a physician.
  • Duration of use: limit to 3–5 days to avoid rebound congestion.
  • Pre‑existing conditions: avoid in patients with narrow‑angle glaucoma or severe hypertension.
  • Concomitant nasal surgery: postpone use until healing is complete.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Nasoryl M can interact with other medications that affect vascular tone or cholinergic pathways.

Major Interactions (Avoid)

  • Systemic alpha‑adrenergic agonists: additive vasoconstrictive effects may raise blood pressure.
  • Other intranasal decongestants: risk of excessive vasoconstriction and rebound congestion.
  • Strong anticholinergic drugs: may increase anticholinergic burden leading to dry mouth or blurred vision.

Moderate Interactions (Monitor Closely):\n- Beta‑blockers: may blunt systemic cardiovascular responses.

  • Antihypertensive agents: monitor blood pressure for potential elevation.
  • Monoamine oxidase inhibitors (MAOIs): observe for hypertensive episodes.

Frequently Asked Questions

Nasoryl M is indicated for relief of nasal congestion and excessive nasal secretions associated with rhinitis, including allergic and non‑allergic forms. It helps open the nasal passages and reduces runny nose, improving breathing comfort.

Xylometazoline Hydrochloride is an alpha‑adrenergic agonist that narrows the blood vessels in the nasal mucosa. This vasoconstriction reduces swelling and edema, leading to faster clearance of the airway and decreased congestion.

The specific dosing regimen for Nasoryl M is determined by the prescribing healthcare professional based on the patient’s age, severity of symptoms, and clinical response. Patients should follow the prescriber’s instructions and not exceed the recommended number of sprays per day.

Safety data for Nasoryl M in pregnancy and lactation are limited. Women who are pregnant, planning to become pregnant, or breastfeeding should discuss potential risks and benefits with their healthcare provider before using the product.

To request Nasoryl M, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any required import documentation.

Unlike single‑agent decongestants, Nasoryl M combines an alpha‑adrenergic vasoconstrictor with an anticholinergic agent, offering both edema reduction and secretory control. This dual mechanism can provide more comprehensive symptom relief for patients with mixed congestion and rhinorrhoea.

Nasoryl M should be stored at room temperature, below 25 °C, in its original packaging. Keep the container tightly closed, protect it from moisture and direct sunlight, and discard any product that appears discoloured or contaminated.

Nasoryl M is delivered as a nasal spray. The patient tilts the head slightly forward, inserts the nozzle into one nostril, and actuates the pump to release the prescribed number of sprays. The same procedure is repeated in the other nostril if directed by the prescriber.

Serious adverse events, though rare, include severe allergic reactions such as anaphylaxis, significant hypertension, nasal ulceration or perforation, and exacerbation of narrow‑angle glaucoma. Any sudden worsening of symptoms should prompt immediate medical evaluation.

Nasoryl M is contraindicated in individuals with known hypersensitivity to xylometazoline, ipratropium, or any excipients in the formulation. It should also be avoided in patients with narrow‑angle glaucoma, severe hypertension, or those who have had recent nasal surgery unless advised by a physician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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