AquaMaster^® (Spray) Instructions for Use

Marketing Authorization Holder

Evalar, CJSC (Russia)

ATC Code

R01AX10 (Other drugs)

Active Substance

Sodium chloride (Ph.Eur. European Pharmacopoeia)

Dosage Form

AquaMaster®

Nasal spray 0.65%: bottle 30 mL or 50 mL

Dosage Form, Packaging, and Composition

Nasal spray as a clear, colorless liquid with a faint characteristic almond odor.

Excipients: benzalkonium chloride, benzyl alcohol, disodium phosphate dodecahydrate, sodium dihydrogen phosphate dihydrate, purified water.

30 ml – glass bottles (1) with a spray nozzle – cardboard packs.
50 ml – glass bottles (1) with a spray nozzle – cardboard packs.

Clinical-Pharmacological Group

Drug for moisturizing, cleansing, and protecting the nasal mucosa

Pharmacotherapeutic Group

Remedy for nasal conditions

Pharmacological Action

It effectively moisturizes the nasal mucosa, thins thick mucus, softens dry crusts in the nose, and facilitates their easy removal.

The pH of the solution is close to the pH of the natural secretory fluid of the nasal mucosa.

Indications

• Administer for daily hygienic care of the nasal cavity in infants, children, and adults.
• Use to cleanse the nasal cavity of accumulated mucus and dried crusts in conditions of dry nasal mucosa.
• Apply as part of the management regimen for rhinitis of various etiologies, including acute, chronic, allergic, and atrophic forms.

ICD codes

Dosage Regimen

Administer intranasally with a frequency of 3 to 4 times per day for both preventive and therapeutic purposes.

Continue the typical treatment and prevention course for a duration of 2 to 4 weeks to achieve optimal cleansing and moisturizing effect.

Ensure the use of an age-appropriate dosage form for young children and infants to guarantee safe and effective administration.

Adverse Reactions

Monitor for local or systemic allergic reactions, which are possible but infrequently reported.

Discontinue use immediately and consult a healthcare professional if any signs of hypersensitivity, such as local irritation, itching, redness, or rash, develop.

Contraindications

• Do not use in patients with a known hypersensitivity to sodium chloride or any of the listed excipients, including benzalkonium chloride and benzyl alcohol.
• Avoid administration in individuals with a history of allergic reactions to any component of the formulation.

Use in Pregnancy and Lactation

Can be used during pregnancy and breastfeeding.

Use in Hepatic Impairment

The drug is approved for use in hepatic impairment.

Use in Renal Impairment

The drug is approved for use in renal impairment.

Pediatric Use

The drug is approved for use in children and adolescents under 18 years of age.

Geriatric Use

The drug is approved for use in elderly patients.

Special Precautions

When used as part of complex therapy, other medicinal products should be administered intranasally after cleansing the nasal cavity – 10-15 minutes after spraying.

Storage Conditions

Store at 15°C (59°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.