Bactericidal recirculator A-40 (40 m2) for home and office, with light

Release form, composition and packaging

Spray for topical application dosed in the form of a colorless transparent liquid with a characteristic mint odor.

1 dose

100 ml

benzydamine hydrochloride

0.255 mg

0.15 g

ethanol 96% - 10 ml, glycerol - 5 g, methyl parahydroxybenzoate - 0.1 g, menthol flavor (flavoring additive) - 0.03 g, saccharin - 0.024 g, sodium bicarbonate - 0.011 g, polysorbate 20 - 0.005 g, purified water - qs up to 100 ml.

30 ml (176 doses) - polyethylene bottles with a pump and a pressure device with a folding cannula (1) - cardboard packs.

pharmachologic effect

NSAIDs for topical use, belongs to the indazole group.

It has anti-inflammatory and local anesthetic effect, has an antiseptic effect against a wide range of microorganisms.

The mechanism of action of the drug is associated with the stabilization of cell membranes and inhibition of prostaglandin synthesis.

Benzydamine has an antibacterial effect due to the rapid penetration of microorganisms through the membranes with subsequent damage to cellular structures, disruption of metabolic processes and cell lysis.

Has antifungal action against Candida albicans.

It causes structural modifications of the cell wall of fungi and the metabolic chains of mycetes and, thus, prevents their reproduction.

This property was the basis for the use of benzydamine in inflammatory processes in the oral cavity, incl.

infectious etiology.

Pharmacokinetics

When applied topically, the drug is well absorbed through the mucous membranes and penetrates into the inflamed tissues, it is found in the blood plasma in an amount insufficient to obtain systemic effects.

Benzydamine is excreted mainly by the kidneys in the form of inactive metabolites or conjugation products.

Indications for use

Symptomatic therapy of pain syndrome of inflammatory diseases of the oral cavity and ENT organs (of various etiology):

gingivitis, glossitis, stomatitis (including after radiation and chemotherapy)

pharyngitis, laryngitis, tonsillitis

candidiasis of the oral mucosa (as part of combination therapy)

calculous inflammation of the salivary glands

after surgical interventions and injuries (tonsillectomy, jaw fractures)

after treatment and tooth extraction

periodontal disease.

For infectious and inflammatory diseases requiring systemic treatment, it is necessary to use Tantum Verde as part of a combination therapy.

Contraindications for use

children under 3 years old

hypersensitivity to benzydamine or other components of the drug.

The drug should be used with caution in case of hypersensitivity to acetylsalicylic acid or other NSAIDs

bronchial asthma (including history).

Dosage regimen

The drug is used topically after meals.

1 dose (1 injection) corresponds to 0.255 mg benzydamine.

Adults (including elderly patients) and children over 12 years of age are prescribed 4-8 injections 2-6 times / day

children aged 6 to 12 years - 4 injections 2-6 times / day

children aged 3 to 6 years - 1 injection for every 4 kg of body weight, but no more than 4 injections (maximum single dose) 2-6 times / day.

Do not exceed the recommended dose.

The duration of treatment should not exceed 7 days.

If after treatment within 7 days there is no improvement or new symptoms appear, the patient should consult a doctor.

Instructions for use

1. Turn the cannula (white tube) vertically to the vial.

2. Insert the cannula into the mouth and direct to the inflamed areas in the mouth or throat.

3. Press the dosing pump on the top of the vial as many times as the prescribed doses.

1 press corresponds to 1 dose.

You must hold your breath during the injection.

Overdose

Currently, no cases of overdose of the drug Tantum Verde have been reported.

When using the drug in accordance with the instructions for use, an overdose is unlikely.

Symptoms: if the drug is accidentally swallowed, the following symptoms are possible - vomiting, abdominal cramps, anxiety, fear, hallucinations, convulsions, ataxia, fever, tachycardia, respiratory depression.

Treatment: carrying out symptomatic therapy

induce vomiting or flush the stomach using a gastric tube (under medical supervision)

medical supervision, supportive therapy and necessary hydration must be provided.

The antidote is unknown.

Side effect

WHO classification of the incidence of side effects: very often (? 1/10)

often (from? 1/100 to < 1/10)

infrequently (from? 1/1000 to < 1/100)

rarely (from? 1/10 000 to < 1/1000)

very rare (< 1/10 000)

frequency unknown (cannot be estimated from available data).

In each group, adverse effects are presented in order of decreasing severity.

Local reactions: rarely - dry mouth, burning sensation in the mouth

frequency unknown - feeling of numbness in the mouth.

Allergic reactions: infrequently - photosensitivity

rarely - hypersensitivity reactions, skin rash, pruritus

very rarely - angioedema, laryngospasm

frequency unknown - anaphylactic reactions.

If any of the side effects indicated in the instructions are aggravated or any other side effects not indicated in the instructions are noted, the patient should immediately inform the doctor about it.

Drug interactions

Interaction studies with other medicinal products have not been conducted.

Application during pregnancy and lactation

The drug Tantum Verde should not be used during pregnancy and during breastfeeding.

special instructions

When using the drug Tantum Verde, hypersensitivity reactions may develop.

In this case, it is recommended to stop treatment and consult a doctor to prescribe appropriate therapy.

In a limited number of patients, the presence of sores in the throat and mouth may indicate a more serious pathology.

If symptoms persist for more than 3 days, the patient should consult a doctor.

The use of Tantum Verde is not recommended in patients with hypersensitivity to acetylsalicylic acid or other NSAIDs.

Tantum Verde should be used with caution in patients with a history of bronchial asthma, because

development of bronchospasm is possible while taking the drug.

Tantum Verde contains parahydroxybenzoates, which can cause allergic reactions.

Influence on the ability to drive vehicles and use mechanisms

The drug does not affect the ability to drive vehicles and work with mechanisms.

Name ENG

TANTUM VERDE

Clinical and pharmacological group

NSAIDs for local use in ENT practice and dentistry.

ATX code

Benzydamine

Dosage

0.255mg / dose x 30ml

Structure

Spray for topical use, dosed 0.255 mg / dose. For 100 ml of spray for topical use, dosed 0.255 mg / dose. Active ingredient: benzydamine hydrochloride - 0.15 g. Excipients: ethanol 96% 10.0 ml, glycerol 5.00 g , methyl parahydroxybenzoate 0.100 g, menthol flavor (flavoring additive) 0.030 g, saccharin 0.024 g, sodium bicarbonate 0.011 g, polysorbate 20 0.005 g, purified water qs up to 100 ml.

Indications

Inflammatory diseases of the oral cavity and ENT organs (of various etiologies): - gingivitis, glossitis, stomatitis (including after radiation and chemotherapy)

- tonsillitis, pharyngitis, laryngitis, tonsillitis

- candidiasis of the oral mucosa (as part of combination therapy)

- calculous inflammation of the salivary glands.

- after surgical interventions and injuries (tonsillectomy, jaw fractures)

- after treatment or tooth extraction

- periodontal disease

For infectious and inflammatory diseases requiring systemic treatment, it is necessary to use Tantum Verde as part of a combination therapy.

Contraindications

hypersensitivity to any of the components of the drug

children under 3 years old

INN / Active ingredient

Benzydamine

Storage conditions and periods

In a dark place at a temperature not exceeding 25 degrees.

Expiration date: 4 years

Specifications

Category

Sore throat

Scope of the medicinal product

Ear, Throat, Nose

Release form

Spray

Manufacturer country

Italy

Package quantity, pcs

one

Vacation conditions

Without recipe

Volume, ml.

30 ml

Brand name

Tantum

Components

cannula

The amount of the dosage form in the primary package

30 ml

Primary packaging type

Polyethylene bottle with a dosing device

Type of consumer packaging

Pack of cardboard

Pharmaco-therapeutic group

NSAIDs

Anatomical and therapeutic characteristics

A01AD02 Benzidamine

Dosage form

Dosed topical spray

Dosage (volume) of the substance in the preparation

0.15 g

Expiration date in days

1460

The target audience

Children

Package weight, g

fifty

Mode of application

:

Spray for topical application, dosed 0.255 mg / dose: < br> < br> Topically, after meals. One dose (one injection) corresponds to 0.255 mg of benzydamine. < br> < br> For adults (including elderly patients) and children over 12 years of age, 4-8 injections 2-6 times a day. Children from 6 to 12 years old - 4 injections 2-6 times a day. Children from 3 to 6 years old: 1 injection for every 4 kg of body weight, but no more than 4 injections (maximum single dose) 2 - 6 times a day. Do not exceed the recommended dose. < br> < br> 1. Rotate the cannula (white tube) to the “vertical to the vial” position. < br> < br> 2. Insert the cannula into the mouth and aim at the inflamed areas in the mouth or throat. < br> < br> 3. Press the dosage pump on the top of the bottle as many times as the prescribed doses.One press corresponds to one dose. Hold your breath while injecting < br> < br> The duration of treatment should not exceed 7 days. If after treatment within 7 days there is no improvement or new symptoms appear, you should consult your doctor. Use the drug only according to the method of administration and in those doses indicated in the instructions. If necessary, please consult your doctor before using the medicinal product.If necessary, please consult your doctor before using the medicinal product.If necessary, please consult your doctor before using the medicinal product. https://translate.google.com/translate?hl=&sl=ru&tl=en&u=https://zz.buy-pharm.com/xzmxa.html;Description

Disinfection area up to 40 m2

Flow capacity - 105 m3 / hour

Total power - 29 W

Supply voltage - 220 V

Mains frequency - 50/60 Hz

Wavelength - 253.7 nm

UV source - bactericidal lamp

Execution - floor

Dimensions (HxWxL) - 400 x 150 x 150 mm

Weight - 1.4 kg

Noise level no more - 37 dB

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Specifications

Manufacturer country

Russia

Dimensions, mm

105 m? / Hour

Item weight, g

1400

Colour

White

Brand name

Statpad

A type

Recirculator

Package weight, g

1800

"