Sanorin Nasal drops 0.1%, 10 ml

Special Price $16.83 Regular Price $17.00
In stock
SKU
FL102038441
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Category

Runny nose

Scope of the medicinal product

Ear, Throat, Nose

Release form

Drops

Manufacturer country

Czech

Package quantity, pcs

one

Description

Release form

Oral drops

pharmachologic effect

The natural physiological microflora of the intestine can be significantly disturbed by such external influences as antibiotic therapy, radiation, stomach surgery, as well as due to inappropriate or unusual nutrition, water changes, climate change and other conditions.

Hilak forte regulates the balance of intestinal microflora and normalizes its composition.

Due to the content of metabolic products of normal microflora in the composition of Hilak Forte, the drug helps to restore normal intestinal microflora in a biological way and allows you to preserve the physiological and biological functions of the intestinal mucosa.

The biosynthetic lactic acid and its buffer salts included in Hilak forte restore the normal value of acidity in the gastrointestinal tract, regardless of whether the patient suffers from high or low acidity.

Against the background of the acceleration of the development of normal intestinal symbionts under the influence of Khilak forte, the natural synthesis of vitamins of the B and K groups is normalized. balance in the intestinal lumen.

There is evidence that Hilak forte enhances the protective functions of the body by stimulating the immune response.

When using Khilak forte, there is an acceleration of the elimination of Salmonella in infants after Salmonella enteritis, which is due to the stimulation of the growth of acidophilic anaerobic intestinal flora and its subsequent antagonistic effect on Salmonella.

Indications

Violation of the physiological flora of the small and large intestine (during and after treatment with antibiotics or sulfonamides, radiation therapy)

digestive insufficiency syndrome, dyspepsia

diarrhea, flatulence, constipation

gastroenteritis, colitis

senile bowel syndrome (chronic, atrophic gastroenteritis)

disorders of the gastrointestinal tract caused by climate change

hypo- and anacid conditions

enterogenic diseases of the gallbladder and liver

allergic skin diseases (urticaria, endogenously caused chronic eczema)

salmonellosis in the stage of convalescence (including infants).

Contraindications

Hypersensitivity to drug components.

Application during pregnancy and lactation

The use of the drug Hilak forte during pregnancy and lactation is considered safe.

However, the decision on the appointment of the drug is made by the attending physician.

special instructions

Concomitant use of this drug with milk and dairy products is not recommended.

Structure

100 ml of the preparation (unflavored / cherry-flavored) contains: active ingredients:

Water substrate of metabolic products

Escherichia coli DSM 4087 * 24.9481 / 24.9481 g

Water substrate of metabolic products

Enterococcus faecalis DSM 4086 * 12.4741 / 12.4741 g

Water substrate of metabolic products

Lactobacillus acidophilus DSM 4149 * 12.4741 / 12.4741 g

Water substrate of metabolic products

Lactobacillus helveticus DSM 4183 * 49.8960 / 49.8960 g

* - substrates contain lactose

excipients: disodium phosphate heptahydrate 1.1590 / 1.1590 g, dipotassium phosphate 1.2650 / 1.2650 g, lactic acid 2.5000-6.2500 / 2.5000-6.2500 g, concentrated phosphoric acid 0 , 3520 / 0.3520 g, potassium sorbate 0.1114 / 0.114 / g, citric acid monohydrate 0.0322 / 0.0322 g, sodium saccharinate - / 0.0200 g, sodium cyclamate - / 0.2000 g, cream flavor - / 0.2000 g, cherry flavor - / 0.5000 g, water up to 100 ml.

Method of administration and dosage

Hilak forte is taken orally before or during a meal, diluted with a small amount of liquid (excluding milk).

The drug is prescribed 3 times a day:

adults: 40-60 drops per appointment

children: 20-40 drops per appointment

babies: 15-30 drops per appointment.

After improvement of the condition, the daily dose can be reduced by half.

Side effects

Hilak forte is well tolerated by patients of any age.

No side effects have been observed to date.

Allergic reactions are possible (skin rash, itching, hives)

constipation, diarrhea.

Drug interactions

Under the influence of antacid drugs, it is possible to neutralize lactic acid, which is part of the Hilak forte drug.

Storage conditions

At a temperature not higher than 25 В° C.

Keep out of the reach of children!

Shelf life

4 years.

After opening the bottle - 6 weeks.

Do not use after the expiration date indicated on the package!

Name ENG

HYLAK FORTE

Clinical and pharmacological group

A drug that regulates the balance of intestinal microflora

ATX code

Antidiarrheal drugs of biological origin, regulating the balance of intestinal microflora

Dosage

etc.

x 100ml

Structure

100 ml of the preparation (unflavored / cherry flavor) contains: active ingredients: Aqueous substrate of metabolic products Escherichia coli DSM 4087 * 24.9481 / 24.9481 g Aqueous substrate of metabolic products Enterococcus faecalis DSM 4086 * 12.4741 / 12.4741 g Water substrate of metabolic products Lactobacillus acidophilus DSM 4149 * 12.4741 / 12.4741 g Water substrate of metabolic products Lactobacillus helveticus DSM 4183 * 49.8960 / 49.8960 g * - substrates contain lactose. auxiliary substances: disodium phosphate heptahydrate 1.1590 / 1.1590 g, dipotassium phosphate 1.2650 / 1.2650 g, lactic acid 2.5000-6.2500 / 2.5000-6.2500 g, phosphoric acid, concentrated 0.3520 / 0.3520 g, potassium sorbate 0.114 / 0.114 / g, citric acid monohydrate 0.0322 / 0.0322 g, sodium saccharinate - / 0.0200 g, sodium cyclamate - / 0.2000 g, cream flavor - / 0.2000 g,cherry flavor - / 0.5000 g, water up to 100 ml.

Indications

violations of the physiological flora of the intestine (during and after treatment with antibiotics, sulfonamides, radiation therapy)

digestive insufficiency syndrome, dyspepsia

diarrhea, flatulence, constipation

gastroenteritis, colitis

senile bowel syndrome (chronic, atrophic gastroenteritis)

disorders of the gastrointestinal tract caused by climate change

hypo- and anacid conditions

enterogenic diseases of the gallbladder and liver

allergic skin diseases (urticaria, endogenously caused chronic eczema)

salmonellosis in the stage of convalescence (including in infants)

Contraindications

Hypersensitivity to drug components

INN / Active ingredient

An embryonic aqueous substrate of metabolic products Streptococcus faevalis DSM 4086 + an embryonic aqueous substrate of metabolic products Lactobacillus acidophilus DSM 4149 + an embryonic aqueous substrate of metabolic products Esherichia coli DSM 4087 + helical non-embryonic aqueous substrate of metabolic products Lveact318

Storage conditions and periods

At a temperature not higher than 25 degrees.

Shelf life: 4 years - vials (6 weeks after opening)

3 years - sachet

Specifications

Scope of the medicinal product

Gastrointestinal tract

Release form

Drops

Manufacturer country

Germany

Package quantity, pcs

one

Scope of application

Gastroenterology

,

Allergology

Minimum age from

From birth

Way of introduction

Through the mouth

Vacation conditions

Without recipe

Shelf life after opening

6 weeks

Volume, ml.

100 ml

Brand name

Hilak forte

The amount of the dosage form in the primary package

100 ml

Primary packaging type

Dark glass bottle

Type of consumer packaging

Pack of cardboard

Pharmaco-therapeutic group

Antidiarrheal agent

Anatomical and therapeutic characteristics

A07FA Antidiarrheal microorganisms

Dosage form

Drops for oral administration

Expiration date in days

1461

The target audience

Adult

Package weight, g

one hundred

Category

:

Preparations for the gastrointestinal tract

,

Dysbacteriosis

,

Probiotics and prebiotics

,

Inulins

Mode of application

:

for adults, the drug is prescribed 40-60 drops 3 times / day < br> children - 20-40 drops 3 times / day < br> infants - 15-30 drops 3 times / day. < br> After improvement of the condition, the initial the daily dose of Hilak forte can be reduced by half. < br> The drug is taken orally before or during meals, diluted in a small amount of liquid, excluding milk.

Dosage (volume) of the substance in the preparation

: https://translate.google.com/translate?hl=&sl=ru&tl=en&u=https://zz.buy-pharm.com/xzecq.html;Description

Sanorin drops called.

0.1% fl.

10ml

Name ENG

SANORIN

Clinical and pharmacological group

A vasoconstrictor drug for local use in ENT practice

ATX code

Naphazoline

Dosage

0.1% x 10ml

Structure

1 ml contains: Active ingredient: naphazoline nitrate 1 mg

Excipients: boric acid, ethylenediamine, methyl parahydroxybenzoate, water.

Storage conditions and periods

In a dark place at a temperature of 10-25 degrees.

Expiration date: 3 years

after opening - 4 weeks

INN / Active ingredient

Naphazoline

Specifications

Category

Runny nose

Scope of the medicinal product

Ear, Throat, Nose

Release form

Drops

Manufacturer country

Czech

Package quantity, pcs

one

Scope of application

Otorhinolaryngology

Minimum age from

2 years old

Way of introduction

Through the respiratory tract

Vacation conditions

Without recipe

Brand name

Teva

The amount of the dosage form in the primary package

10 ml

Primary packaging type

Bottle

Type of consumer packaging

Pack of cardboard

Pharmaco-therapeutic group

Decongestant - alpha adrenergic agonist

Anatomical and therapeutic characteristics

R01AA08 Naphazoline

Dosage form

Nasal drops

Packaging

Box

Dosage (volume) of the substance in the preparation

naphazoline nitrate 1 mg

The target audience

Adult

Expiration date in days

1461

Package weight, g

2

Mode of application

:

In acute rhinitis, sinusitis, eustachitis, laryngitis, to facilitate rhinoscopy Children over 2 years old - 1-2 drops of 0.05% nasal drops in each nasal passage 2-3 times a day with an interval of at least 4 hours. The course of treatment is short-term, until the symptoms of nasal congestion disappear, but not more than 1 week in adults and 3 days in children.

Re-use of the drug is possible after a few days.

In case of nosebleeds, a cotton swab moistened with 0.05% Sanorin solution can be placed in the nasal passage.

As an additional agent in the treatment of conjunctivitis of bacterial origin, nasal drops 0.05% are instilled into the conjunctival sac, 1-2 drops 3-4 times a day.

"

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