Tonsilgon N tab. p / o No. 50
Scope of the medicinal product
The immune system
Release form
Tablet
Manufacturer country
Germany
Package quantity, pcs
fifty
Scope of application
Pulmonology
Release form
Tonsilgon.
Dragee light blue, round, biconvex.
pharmachologic effect
Herbal antiseptic.
Pharmacological properties are due to biologically active substances that make up the drug.
Tonsilgon N has anti-inflammatory and antiseptic properties.
The active components of chamomile, marshmallow and horsetail included in the preparation help to increase the activity of nonspecific factors of the body's defense.
Polysaccharides, essential oils and flavonoids of chamomile, marshmallow and yarrow, oak bark tannins have an anti-inflammatory effect and help reduce swelling of the respiratory tract mucosa.
Indications
Acute and chronic diseases of the upper respiratory tract (tonsillitis, pharyngitis, laryngitis).
Prevention of complications in respiratory viral infections and as an addition to antibiotic therapy for bacterial infections.
Contraindications
Hypersensitivity to the components of the preparation, in particular, to plants of the Asteraceae family
children under 6 years old
for patients with a rare hereditary form of lactose intolerance, fructose intolerance, lactase deficiency, glucose-galactose malabsorption or sucrase-isomaltase deficiency, the use of the drug is contraindicated (due to the content of lactose and sucrose in the drug).
Application during pregnancy and lactation
The use of the drug is possible if the potential benefit to the mother outweighs the potential risk to the fetus and child.
A doctor's consultation is required.
special instructions
If, when using the drug for 7 days, the symptoms of the disease persist or the patient's condition worsens, you should consult a doctor.
One dragee contains less than 0.03 bread units" (XE).
Impact on the ability to drive vehicles and other mechanisms that require increased concentration
The use of the drug does not affect the ability to perform potentially hazardous activities requiring increased concentration of attention and speed of psychomotor reactions.
Structure
1 tablet contains:
Active ingredients: Marshmallow roots 8.0 mg, Chamomile flowers 6.0 mg, Horsetail herb 10.0 mg, Walnut leaves 12.0 mg, Yarrow herb 4.0 mg, Oak bark 4.0 mg, Dandelion herb 4 , 0 mg.
Excipients: lactose 51.523 mg, maize starch 23.290 mg, potato starch 5.858 mg, stearic acid 2.600 mg, glucose monohydrate 0.929 mg, highly dispersed silicon dioxide 0.650 mg.
Dragee coating: calcium carbonate 4.339 mg, glucose syrup 1.536 mg, indigotin 0.002 mg, maize starch 1.240 mg, modified maize starch 3.785 mg, montan glycol wax 0.130 mg, poly (1-vinyl-2-pyrrolidone) K 25 0.112 mg, poly (1-vinyl-2-pyrrolidone) K 30 0.246 mg, castor oil 0.057 mg, sucrose 62.198 mg, shellac 1.476 mg, talc 52.687 mg, highly dispersed silicon dioxide 0.986 mg, titanium dioxide 1.206 mg.
Method of administration and dosage
Inside.
Dragee is swallowed whole, without chewing, if necessary, washed down with water.
In the acute period of the development of the disease
Adults: 2 tablets 5 - 6 times a day.
School-age children (over 6 years old): 1 tablet 5-6 times a day.
After the disappearance of acute symptoms of the disease (sore throat), treatment with the drug should be continued for another 1 week.
After the disappearance of acute symptoms
Adults: 2 tablets 3 times a day.
School-age children (over 6 years old): 1 tablet 3 times a day.
Side effects
From the gastrointestinal tract are possible: nausea, vomiting.
Possible: allergic reactions.
If signs of an allergic reaction appear, you should stop taking the drug.
Drug interactions
The combination with antibacterial drugs is possible and advisable.
Interaction with other medicinal products has not been described.
Overdose
To date, no cases of overdose have been reported.
Symptoms: in case of an overdose, side effects from the gastrointestinal tract may increase.
Treatment: symptomatic.
Storage conditions
The drug should be stored in a dry, dark place, out of the reach of children, at a temperature not exceeding 25 В° C.
Shelf life
3 years.
Active substance
Althea kor., Chamomile color., Horsetail tr., Gretz.
walnut leaf, Yarrow tr., Oak bark., Dandelion tr.
Name ENG
TONSILGON N
Clinical and pharmacological group
Plant antiseptic
ATX code
Other drugs
Dosage
1 tablet: Althea roots 8.0 mg, Chamomile flowers 6.0 mg, Horsetail herb 10.0 mg, Walnut leaves 12.0 mg, Yarrow herb 4.0 mg, Oak bark 4.0 mg, Dandelion herb 4 , 0 mg.
Structure
1 tablet contains: Active ingredients: Marshmallow roots 8.0 mg, Chamomile flowers 6.0 mg, Horsetail grass 10.0 mg, Walnut leaves 12.0 mg, Yarrow grass 4.0 mg, Oak bark 4.0 mg, Dandelion herb 4.0 mg. Excipients: lactose 51.523 mg, maize starch 23.290 mg, potato starch 5.858 mg, stearic acid 2.600 mg, glucose monohydrate 0.929 mg, highly dispersed silicon dioxide 0.650 mg Dragee shell, calcium carbonate 4.339 mg syrup 1.536 mg, indigotin 0.002 mg, maize starch 1.240 mg, modified maize starch 3.785 mg, montan glycol wax 0.130 mg, poly (1-vinyl-2-pyrrolidone) K 25 0.112 mg, poly (1-vinyl-2-pyrrolidone) K 30 0.246 mg, castor oil 0.057 mg, sucrose 62.198 mg, shellac 1.476 mg, talc 52.687 mg, highly dispersed silicon dioxide 0.986 mg, titanium dioxide 1.206 mg.
Indications
Acute and chronic diseases of the upper respiratory tract (tonsillitis, pharyngitis, laryngitis). Prevention of complications in respiratory viral infections and as an addition to antibiotic therapy for bacterial infections.
INN / Active ingredient
Marshmallow roots, Chamomile flowers, Horsetail herb, Walnut leaves, Yarrow herb, Oak bark, Dandelion herb
Storage conditions and periods
At a temperature not exceeding 25 degrees, in the original packaging.
Expiration date: 3 years
Contraindications
hypersensitivity to the components of the preparation, in particular, to plants of the Asteraceae family
children under 6 years old
for patients with a rare hereditary form of lactose intolerance, fructose intolerance, lactase deficiency, glucose-galactose malabsorption or sucrase-isomaltase deficiency, the use of the drug is contraindicated (due to the content of lactose and sucrose in the drug).
Specifications
Scope of the medicinal product
The immune system
Release form
Tablet
Manufacturer country
Germany
Package quantity, pcs
fifty
Scope of application
Pulmonology
Minimum age from
6 years
Way of introduction
Through the mouth
Vacation conditions
Without recipe
Brand name
Bionorica
The amount of the dosage form in the primary package
25 pcs.
Primary packaging type
Blister
Type of consumer packaging
Pack of cardboard
Pharmaco-therapeutic group
Herbal immunostimulating agent
Anatomical and therapeutic characteristics
R02AA20 Other antiseptics
Dosage form
Film-coated tablets
Packaging
Cardboard box
The target audience
Children
Expiration date in days
1095
Package weight, g
45
Category
:
Antibiotics
,
Antiseptics and disinfectants
,
Disinfectants
Mode of application
:
Inside.
Dragees are swallowed whole, without chewing, washed down with water if necessary. < br> In the acute period of the development of the disease. Adults: 2 tablets 5 - 6 times a day. < br> School-age children (over 6 years old): 1 tablet 5 - 6 times a day. < br> After the disappearance of acute symptoms of the disease (sore throat), you should continue treatment with the drug for another 1 week. < br> After the disappearance of acute symptoms < br> Adults: 2 tablets 3 times a day. < br> Children of school age (over 6 years old): 1 tablet 3 times a day. < br>
Dosage (volume) of the substance in the preparation
:
1 tablet: Althea roots 8.0 mg, Chamomile flowers 6.0 mg, Horsetail herb 10.0 mg, Walnut leaves 12.0 mg, Yarrow herb 4.0 mg, Oak bark 4.0 mg, Dandelion herb 4 , 0 mg.
Information on technical characteristics, delivery set, country of manufacture "