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Ingalipt-N oral spray can 30 g

Brand: ТОВ «Мікрофарм» SKU: an-1850
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Ingalipt-N oral spray can 30 g
Ingalipt-N oral spray can 30 g
Ingalipt-N oral spray can 30 g
Ingalipt-N oral spray can 30 g
Ingalipt-N oral spray can 30 g
Ingalipt-N oral spray can 30 g
In Stock
157.04 грн.
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Active ingredient:Sulphathiazole, Sulfanilamide
Adults:Can
ATC code:R RESPIRATORY SYSTEM AGENTS; R02 THROAT DISEASES PREPARATIONS; R02A THROAT DISEASES PREPARATIONS; R02A A Antiseptics; R02A A20 Miscellaneous antiseptics
Country of manufacture:Ukraine
Diabetics:Can
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Ingalipt-N oral spray can 30 g
157.04 грн.
Description

Instructions for Ingalipt-N oral spray, canister 30 g

Composition

active ingredients: soluble streptocide, sodium sulfathiazole hexahydrate;

1 cylinder contains soluble streptocide 0.75 g, sodium sulfathiazole hexahydrate 0.75 g;

excipients: thymol, peppermint oil, eucalyptus oil, glycerin, ethanol 96%, polysorbate 80, sucrose, purified water.

Dosage form

Oral spray.

Main physicochemical properties: transparent liquid from light yellow to dark yellow in color with a specific odor.

Pharmacotherapeutic group

Means acting on the respiratory system. Drugs used for throat diseases. Antiseptics. Various antiseptics.

ATX code R02A A20.

Pharmacological properties

Pharmacodynamics

Ingalipt-N has antibacterial and anti-inflammatory effects, as well as a cooling and distracting effect. The combination of these pharmacological properties provides a comprehensive pathogenetic therapy for inflammatory diseases of the upper respiratory tract and oral mucosa. Ingalipt-N does not have an ulcerogenic or general toxic effect on the body.

Pharmacokinetics

Ingalipt-N is intended for local inhalation use and creates a therapeutic concentration mainly in the focus of inflammation. Sulfonamides (soluble streptocide and sodium norsulfazole) are partially absorbed into the systemic bloodstream, which reversibly bind to blood proteins: soluble streptocide - by 12–14%, sodium norsulfazole - by 55%. In the process of biotransformation, acetylated forms of sulfonamides are formed, in which form they are excreted by the kidneys. The half-life of soluble streptocide is 10 hours, sodium norsulfazole - 1.2 hours.

Indication

Local treatment of infectious and inflammatory diseases of the ENT organs and the oral mucosa (tonsillitis, pharyngitis, laryngitis, aphthous and ulcerative stomatitis).

Contraindication

Hypersensitivity to the components of the drug, history of severe toxic-allergic reactions to sulfonamides.

Interaction with other medicinal products and other types of interactions

If you are taking any other medications, be sure to consult your doctor about the possibility of further use of the drug!

The antimicrobial effect of the drug may be weakened when used simultaneously with drugs that are derivatives of para-aminobenzoic acid (novocaine, anestezin, dicaine).

Application features

Before using the drug, people with a tendency to allergies should consult a doctor!

Do not use the drug beyond the prescribed period without consulting a doctor!

Be sure to inform your doctor about any previous reactions to taking drugs in this group.

Do not allow the drug to get into the eyes.

Before first use, press the nozzle up to 7 times until a dispersed jet appears. If there is no jet, you can repeat the steps again.

Before using the drug, it is recommended to rinse the oral cavity with warm boiled water. Remove necrotic plaque from the affected areas of the oral cavity (ulcers, erosions) using sterile swabs.

After irrigating the oral cavity with the drug, you should refrain from eating for 15–30 minutes.

After using the drug, remove the throat spray from the stem and rinse it with warm water. Close the bottle with a protective cap to prevent its contamination.

When using the drug in children, it should be taken into account that a single dose of the drug, which is sprayed in 1–2 sprays, contains 0.0076–0.0152 ml of ethanol (96%), which is 0.0004–0.0013 ml/kg per single dose for children aged 3–5 years (body weight 15–21 kg), 0.0002–0.0007 ml/kg for children aged 6–12 years (body weight 21–38 kg).

As the medicinal product contains sucrose, patients with rare hereditary problems of fructose intolerance, glucose-galactose malabsorption or sucrase-isomaltase insufficiency should not take this medicine.

Ability to influence reaction speed when driving vehicles or other mechanisms

The drug does not affect the ability to drive vehicles and mechanisms, however, drivers should consider the possible distortion of the results of alcohol tests.

Use during pregnancy or breastfeeding

The use of the drug during pregnancy or breastfeeding is possible under the supervision of a doctor after an assessment, weighing the benefit/risk ratio with strict adherence to the dosage regimen.

Method of administration and doses

Apply to adults and children over 3 years of age topically on the mucous membranes of the oral cavity and nasopharynx by irrigation.

Adults should irrigate 3–4 times a day.

For children aged 3 and over, irrigation should be performed 1–2 times a day, unless otherwise directed by a doctor.

The duration of use of the drug depends on the course of the disease and is usually 3–10 days.

The frequency and duration of use are determined individually by the doctor and depend on the severity of the disease!

The drug should not be used in children under 3 years of age. Use with caution in children over 3 years of age due to the possibility of reflex bronchospasm due to the content of eucalyptus and peppermint essential oils. Treatment of children should be carried out under the supervision of a physician.

Overdose

Cases of overdose have not been described. Possible increase in side effects.

Treatment: discontinuation of the drug, rinsing the mouth with warm boiled water.

Therapy is symptomatic.

Adverse reactions

Immune system disorders: allergic reactions, including angioedema, bronchospasm.

Skin: rash, itching, urticaria, swelling at the site of contact.

On the part of the digestive system: nausea, vomiting, local effects (burning in the mouth, lump in the throat or irritation).

Others: general weakness, difficulty breathing.

If any adverse events or unusual reactions are detected, you should consult a doctor regarding further use of the drug.

Expiration date

2 years.

It is forbidden to use the medicine after the expiration date indicated on the package.

Storage conditions

Store at a temperature not exceeding 25 ° C. Keep out of the reach of children, away from fire.

Packaging

30 g in an aluminum can with a sprayer and a protective cap.

Vacation category

Without a prescription.

Producer

LLC "Micropharm".

Location of the manufacturer and its business address

Ukraine, 61013, Kharkiv, Shevchenko St., 20.

Specifications
Characteristics
Active ingredient
Sulphathiazole, Sulfanilamide
Adults
Can
ATC code
R RESPIRATORY SYSTEM AGENTS; R02 THROAT DISEASES PREPARATIONS; R02A THROAT DISEASES PREPARATIONS; R02A A Antiseptics; R02A A20 Miscellaneous antiseptics
Country of manufacture
Ukraine
Diabetics
Can
Drivers
Can
For allergies
With caution
For children
From 3 years old
Form
Sprays
Method of application
For the oral cavity
Nursing
Under the supervision of a doctor
Pregnant
By doctor's prescription
Producer
Micropharm LLC
Quantity per package
30 ml
Series/Line
For children
Trade name
Ingalipt
Vacation conditions
Without a prescription
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