INSTRUCTIONS for medical use | consumption | of the medicinal product AQUAMAX (AQUAMAX)

Composition:

Active substance: 1 ml of the preparation contains sodium chloride 6.5 mg;

Excipients: benzalkonium chloride, anhydrous sodium dihydrogen phosphate, anhydrous sodium hydrogen phosphate, purified water.

Pharmaceutical form. Nasal drops.

Main physicochemical properties: clear colorless liquid.

Pharmacotherapeutic group. Preparations used in diseases of the nasal cavity.

ATC code R01AX10.

Pharmacological properties.

Effectively moisturizes the nasal mucosa, dilutes thick mucus, softens dry nasal crusts, and facilitates their easy removal.

Highly purified stabilized 0.65% sodium chloride solution closely matches natural nasal secretion. Buffering agents contained in the formulation adjust the solution's pH to that of the natural secretory fluid of the nasal mucosa and maintain this parameter at a constant level.

Aquamax improves olfactory perception and ciliary epithelium transport function, promotes restoration of nasal breathing, shortens the rehabilitation period, and allows reduction in dosage and frequency of use of locally acting vasoconstrictive agents.

Clinical characteristics.

Indications. Used for infants, children, and adults:

for hygienic care of the nasal cavity, prevention and complex treatment of diseases of the nasal mucosa and paranasal sinuses associated with dryness of the nasal mucosa or mucus formation (atrophic, allergic, infectious, drug-induced rhinitis);
as an adjunctive agent when using local vasoconstrictive agents;
to relieve dryness of the nasal mucosa caused by air conditioning systems, including automotive air conditioners, or central heating radiators, during air flights;
after surgical interventions in the nasal cavity and nasal sinuses.

Contraindications. Hypersensitivity to the components of the product.

Interaction with other medicinal products and other types of interactions. Not described.

Instructions for use.

To avoid the spread of infection, it is recommended that the bottle with dropper be used individually.

Use during pregnancy or breastfeeding. Without restrictions.

Ability to affect reaction speed when driving or operating machinery. No effect.

Method of administration and dosage. Adults – 2 drops, children aged 1 year and older – 1–2 drops, children under 1 year – 1 drop in each nostril 3–4 times daily for therapeutic purposes; for hygienic purposes – 1–4 times daily.

Children. Use in children should be under adult supervision.

Overdose. Cases of overdose, as well as any toxic or systemic reactions following the use of Aquamax, have not been reported.

Adverse reactions.

Allergic reactions are possible in individuals with hypersensitivity to the components of the drug.

Shelf life. 3 years.

Storage conditions. Store in the original packaging at a temperature not exceeding 25 °C. Keep out of the reach of children.

Packaging. 20 ml in a bottle closed with a dropper cap and pipette, in a box.

Category of supply|release|. Over-the-counter.

Manufacturer. LIMITED LIABILITY COMPANY "CORPORATION "ZDOROVIYA".

Manufacturer's address and location of business activity.

22 Shevchenko Street, Kharkiv, Kharkiv region, 61013, Ukraine.