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Dosage form: & nbspgel dental
Composition:

100 g of the preparation contain:

Active substances:

Metronidazole - 1.00 g

Chlorhexidine (chlorhexidine bigluconate solution 20%) - 0.50 g

Auxiliary substances:

Levomentola (L-Menthol) 0.25 g

Glycerol (glycerin distilled) - 5.00 g

Propylene glycol 5.00 g

Trolamine (thermostable triethanolamine) 0.47 g

Carbomer - 1.25 g

Sodium saccharinate dihydrate 0.25 g

Waters purified - 86.28 grams

Description:

Homogeneous gel, from white to white with a yellowish hue of color.

Pharmacotherapeutic group:Antimicrobial agent
ATX: & nbsp
  • Antimicrobials for topical use in diseases of the oral cavity
  • Pharmacodynamics:

    Combined antimicrobial preparation. The effectiveness of the drug is due to the presence in its composition of active ingredients, such as metronidazole and chlorhexidine.

    Metronidazole - a derivative of nitroimidazole, which has antiprotozoal and antibacterial action against anaerobic protozoa and anaerobic bacteria that cause periodontitis: Porphyromonas gingivalis, Prevotella intermedia, Prevotella denticola, Fusobacterium fusiformis, Wolinella recta, Treponema spp., Eikenella corrodens, Borrelia vincenti, Bacteroides melaninogenicus, Selenomonas spp. Inactive against aerobic bacteria. The mechanism of action is the biochemical reduction of the 5-nitro group of metronidazole by intracellular transport proteins of anaerobic microorganisms and protozoa.The reduced 5-nitro group of metronidazole reacts with the DNA of a cell of microorganisms, inhibiting the synthesis of their nucleic acids, which leads to the death of bacteria.

    Chlorhexidine - a disinfectant, active against a wide range of vegetative forms of gram-negative and gram-positive microorganisms, yeast, dermatophytes and lipophilic viruses. On bacterial spores acts only at elevated temperature. The bactericidal effect is due to cation binding (the result of dissociation salts of chlorhexidine in a physiological environment) with negatively charged walls of bacterial cells and extramicrobial complexes. In low concentrations, disrupting the osmotic equilibrium of bacterial cells and the release of K + and phosphorus from them, has a bacteriostatic effect; at high cytoplasmic concentrations: the contents of the bacterial cell are deposited, leading ultimately to the death of bacteria.

    Pharmacokinetics:

    With topical application, the Dentamet gel is not practically absorbed.

    Indications:

    Infectious-inflammatory diseases of periodontal and oral mucosa:

    - acute (disruption of normal gum function, bleeding, ulceration) and chronic (proliferation of gum tissue) gingivitis;

    - acute ulcerous-necrotic gingivitis of Vincent (rapid necrosis of soft tissues of the oral cavity);

    - acute (as a result of trauma in orthopedic treatment) and chronic (overhanging edges of seals, abundant dental deposits, defects in prosthetics of teeth, pathology of occlusion) periodontitis;

    - juvenile periodontitis (an inflammatory disease that occurs in adolescents aged 10-13 years);

    - periodontal disease complicated by gingivitis;

    - aphthous stomatitis (oval or round mucosa defects);

    - cheilitis (defeat of the lips in the form of their pallor, maceration with transverse cracks and bright red border on the line of closure of the lips),

    - postextraction alveolitis (inflammation of the hole after tooth extraction);

    - periodontitis (swelling of the fixed part of the gum resulting from bacterial inflammation and impaired draining of the gingival pocket);

    - periodontal abscess (as part of combination therapy).

    Contraindications:

    Individual intolerance to metronidazole, chlorhexidine, as well as derivatives of nitroimidazole.Dentamet is not recommended for use in children under the age of 6 due to insufficient data on efficacy and safety.

    Carefully:

    Pregnancy, lactation.

    Pregnancy and lactation:It is not recommended to prescribe the drug to pregnant women in the first trimester of pregnancy. During the lactation period, the issue of stopping breastfeeding should be addressed.
    Dosing and Administration:

    Locally, for dental use.

    Adults and children over 6 years.

    Dentamet is applied to the affected area of ​​the oral mucosa 2 times a day. The duration of treatment is an average of 7-10 days. It is not recommended to wash off the gel. After applying the gel, you should refrain from drinking and eating for 30 minutes.

    To prevent exacerbations of chronic gingivitis and periodontitis, Dentamet gel is applied to the gum area 2 times a day for 7-10 days. Preventive courses of treatment are carried out 2-3 times a year.

    For prevention of postextraction alveolitis after tooth extraction, the well is treated with Dentamet gel, then the gel is applied on an outpatient basis 2-3 times a day for 7-10 days.

    Side effects:

    With the local application of the Dentamet gel, the risk of developing systemic side effects is small, but sometimes there may be: "metallic" taste in the mouth, headache, allergic reactions (skin rash, itching, urticaria).

    If any of the side effects listed in the manual are aggravated, or if you notice other side effects not indicated in the instructions, tell your doctor.

    Overdose:

    There were no cases of drug overdose with topical application.

    Interaction:

    At local application in recommended doses of systemic interaction of gel Dentamet with other medical products it is not revealed.

    Special instructions:

    Avoid contact with eyes.

    Application of the gel Dentamet does not replace hygienic cleaning of teeth, therefore during the course of treatment with the drug, the cleansing should be continued.

    Effect on the ability to drive transp. cf. and fur:

    There is no evidence of adverse effects.

    Form release / dosage:

    Dental gel.

    Packaging:

    By 10 or 25 g in an aluminum tube with a bud. Each tube together with the instruction for use is placed in a pack of cardboard.

    Storage conditions:
    In the dark place at a temperature of no higher than 25 FROM.
    Keep out of the reach of children.
    Shelf life:

    2 years. Do not use after the expiry date printed on the package.

    Terms of leave from pharmacies:Without recipe
    Registration number:LS-000237
    Date of registration:24.05.2010
    Expiration Date:Unlimited
    The owner of the registration certificate:ALTAYVITAMINS, CJSC ALTAYVITAMINS, CJSC Russia
    Manufacturer: & nbsp
    Information update date: & nbsp23.03.2017
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