Bobotik drops d / vn. receiving fl.-cap. dark glasses 66.66 mg / ml 30ml №1

Release form, composition and packaging

?

Drops for oral administration in the form of a thick opaque liquid from white to creamy white with a fruity odor

separation into a liquid layer and sediment is allowed, which, after shaking, form a homogeneous emulsion.

1 ml

simethicone 66.66 mg

in the form of a 30% emulsion 222.2 mg

sodium saccharinate, methyl parahydroxybenzoate, propyl parahydroxybenzoate, sodium carmellose, citric acid monohydrate, raspberry flavor, purified water.

30 ml - dark glass vials with a polyethylene dropper stopper and a plastic screw cap (1) - cardboard packs.

pharmachologic effect

A drug that reduces flatulence. Simethicone (activated dimethicone) is a combination of methylated linear siloxane polymers stabilized by trimethylsiloxyl groups with silicon dioxide. Reducing the surface tension at the interface makes it difficult to form and promotes the destruction of gas bubbles in the contents of the intestine and gastrointestinal mucus. The gases released during this can be absorbed by the intestinal walls or excreted due to peristalsis. This prevents the formation of large gas-mucous conglomerates, causing painful bloating. During sono- and radiography, it prevents the occurrence of image defects promotes better irrigation of the colon mucosa with contrast agents, preventing the rupture of the contrast film.Due to its chemical inertness, it does not affect microorganisms and enzymes present in the digestive tract. Does not reduce food absorption, does not change the reaction and volume of gastric juice.

Pharmacokinetics

After oral administration, simethicone is not absorbed from the gastrointestinal tract and is excreted through the intestines unchanged.

Indications for use

- increased gas formation and accumulation of gases in the gastrointestinal tract (colic, feeling of fullness in the abdominal cavity, flatulence (including in the postoperative period), Remgeld's syndrome, aerophagia)

- preparation for diagnostic examinations of the abdominal cavity and small pelvis organs (X-ray, sonography, gastroscopy and duodenoscopy - to prevent foam formation).

Contraindications for use

- intestinal obstruction

- obstructive gastrointestinal diseases

- newborns up to 28 days of age

- hypersensitivity to simethicone and / or other components of the drug.

Dosage regimen

The drug is administered orally, after meals. Before use, the bottle should be shaken until a homogeneous emulsion is obtained. For accurate dosage of the drug during instillation, the bottle should be held vertically. With increased gas formation and accumulation of gases in the gastrointestinal tract, children from 28 days of age to 2 years are prescribed 8 drops (20 mg of simethicone) 4 times / day children from 2 to 6 years old - 14 drops (35 mg of simethicone) 4 times / day children over 6 years old and adults - 16 drops (40 mg of simethicone) 4 times / day. For more convenient administration of the drug, in particular to small children, it can be pre-mixed with a small amount of cold boiled water, baby food or non-carbonated liquid. After the symptoms disappear, the drug should be discontinued.In preparation for diagnostic procedures (X-ray examination of the gastrointestinal tract), 1 day before the study, the drug is prescribed 2 times / day (morning and evening): children from 28 days of life to 2 years old - 10 drops (25 mg), children from 2 to 6 years old - 16 drops (40 mg), children over 6 years old and adults - 20 drops (50 mg). For a sonographic study of the gastrointestinal tract, 1 day before the study, the drug is prescribed 2 times / day (morning and evening) in dosages recommended in preparation for an X-ray study. The dose should be repeated 3 hours before the start of the study.For a sonographic study of the gastrointestinal tract, 1 day before the study, the drug is prescribed 2 times / day (morning and evening) in dosages recommended in preparation for an X-ray study. The dose should be repeated 3 hours before the start of the study.For a sonographic study of the gastrointestinal tract, 1 day before the study, the drug is prescribed 2 times / day (morning and evening) in dosages recommended in preparation for an X-ray study. The dose should be repeated 3 hours before the start of the study.

Overdose

There are no reports of overdose.

Simethicone is not absorbed from the gastrointestinal tract and an overdose does not pose a threat to life and health.

Side effect

The development of allergic reactions is possible.

Drug interactions

Name ENG

BOBOTIK

Clinical and pharmacological group

A drug that reduces flatulence

ATX code

Silicones

Dosage

66.66mg / ml x 30ml

Structure

1 ml of oral drops contains: active ingredients: simethicone emulsion 30% 222.2 mg, simethicone 66.66 mg

excipients: sodium saccharinate, methyl parahydroxybenzoate, propyl parahydroxybenzoate, sodium carmellose, citric acid monohydrate, raspberry flavor, purified water

Indications

Increased gas formation and accumulation of gases in the gastrointestinal tract (colic, feeling of fullness in the abdominal cavity, flatulence / including in the postoperative period /, Remgeld's syndrome, aerophagia)

preparation for diagnostic examinations of the abdominal cavity and small pelvis organs (X-ray, sonography, gastroscopy and duodenoscopy - to prevent foam formation).

Contraindications

Hypersensitivity, intestinal obstruction, obstructive gastrointestinal conditions.

INN / Active ingredient

simethicone

Storage conditions and periods

At a temperature not higher than 25 degrees.

Expiration date: 2 years

Specifications

Category

Flatulence

Scope of the drug

Gastrointestinal tract

Release form

Drops

Manufacturer country

Poland

Package quantity, pcs

one

Minimum age from

From birth

Way of introduction

Through the mouth

Vacation conditions

Without recipe

Volume, ml.

30 ml

Brand name

Akrikhin

The amount of the dosage form in the primary package

30 ml

Primary packaging type

Dark glass dropper bottle

Type of consumer packaging

Pack of cardboard

Pharmaco-therapeutic group

Carminative

Dosage form

Drops for oral administration

The target audience

Children

Dosage (volume) of the substance in the preparation

66.66 mg

Expiration date in days

730

Package weight, g

80

Mode of application

:

Bobotik is prescribed inside, after eating. < br> Before use, the bottle should be shaken until a homogeneous emulsion is obtained. < br> For accurate dosage of the drug during instillation, the bottle should be held vertically. < br> With increased gas formation and accumulation of gases in the gastrointestinal tract, children from 28 days life up to 2 years is prescribed 8 drops (20 mg of simethicone) 4 times / day

children from 2 to 6 years old - 14 drops (35 mg of simethicone) 4 times / day

children over 6 years old and adults - 16 drops (40 mg of simethicone) 4 times / day < br> For more convenient administration of BOBOTIK, in particular for small children, it can be pre-mixed with a small amount of cold boiled water, baby food or non-carbonated liquid.

After the symptoms disappear, the drug should be discontinued.

Anatomical and therapeutic characteristics

:

A03AX Drugs for the treatment of intestinal disorders other

Information on technical characteristics, delivery set, country of manufacture