Dologal ST (Dologel ST)

Composition Pharmacodynamics Indications Carefully Contraindications Dosing and Administration Side effects Form release / dosage
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Dosage form: & nbsp

gel stomatologic.

Composition:
Each 10 g contains:
active substances: choline salicylate solution - 1.74 g (equivalent to 0.87 g choline salicylate), benzalkonium chloride (50% solution, equivalent to 0.0005 g benzalkonium chloride) - 0.001 g,lidocaine hydrochloride (in the form of lidocaine hydrochloride monohydrate) -0.2 g;
Excipients: carbomer-934, methyl parahydroxybenzoate,
propyl parahydroxybenzoate, sodium saccharinate, polysorbate 60, levomenthol, propylene glycol, trolamine, glycerol, anethole, Bitter Mask flavor (prpylene glycol, orange oil, vanillin, ethylvaniline, diethyl malonate, maltol, furaneol), purified water.
Description:From a colorless to light brown color, a homogeneous gel with an anise smell. Possibility of opalescence
Pharmacotherapeutic group:nonsteroidal anti-inflammatory drug
ATX: & nbsp
  • Other preparations for topical use in diseases of the oral cavity
    • Pharmacodynamics:
    Combined drug with local anesthetic, antiseptic and anti-inflammatory effect.
    Choline salicylate. Anti-inflammatory: It has antipyretic, anti-inflammatory and analgesic effect. The spectrum of antimicrobial action includes Gram-positive and Gram-negative microorganisms, some fungi and viruses. The action develops in 2-3 minutes and lasts 2-3 hours.
    Benzalkonium chloride.Antiseptic, also has an antifungal, antiprotozoal effect, inactivates the herpes virus. It shows bactericidal activity against staphylococci, streptococci, gram-negative bacteria (intestinal and pseudomonas aeruginosa, proteus, klebsiella, etc.), anaerobic bacteria, fungi and molds. It acts on strains of bacteria resistant to antibiotics and other chemotherapeutic drugs; suppresses plasmacoagulase and hyaluronidase of staphylococci. Does not affect the normal microflora. Virtually not absorbed with topical application.
    Lidocaine. Local anesthetic of amide type. Provides local anesthesia by blocking the formation and passage of a nerve impulse. The mechanism of action is associated with Stabilization of the membrane permeability of neurons for sodium ions. The action of lidocaine develops within 1 min. The attained decrease in sensitivity slowly disappears within 30-60 minutes. With topical application on the mucous membranes lidocaine absorbed moderately.
    The optimal antimicrobial action and adequate analgesia develop 5-10 min after the application of Dologel ® ST.
    Indications:
    Dologel® ST is used as a local painkiller, antiseptic and anti-inflammatory agent under the following conditions:
    -toothache;
    - damage to the oral mucosa (corns, ulcers, wounds);
    - infectious-inflammatory, ulcerative-necrotic and trophic diseases of the oral mucosa;
    - periodontal disease;
    - Postoperative period after small operative interventions in the oral cavity.
    Contraindications:
    Hypersensitivity to any of the components of the drug.
    Pregnancy, lactation (lactation), children's age (under 18), due to the lack of data on the safety of the drug during these periods.
    Pregnancy and lactation:Contraindicated use.
    Dosing and Administration:
    Locally, a small amount of gel (about 10 mm) is applied to the tip of a pure index finger and gently rubbed into the inflamed area 3-4 times a day, or with the help of a dentist, with light massaging movements.
    When treating periodontal diseases, enter into the gingival pockets or gently rub into the inflamed gums 1-2 times a day, as well as in the form of an application or periodontal bandage.
    Side effects:Rarely - allergic reactions, burning sensation in the place of application.
    Overdose:Cases of overdose with local dental use are unknown.
    Interaction:

    Avoid joint use with iodine preparations.

    Monoamine oxidase (MAO) inhibitors enhance the local anesthetic effect of lidocaine.

    The drug is incompatible with soap and detergents containing an anionic group (saponins, sodium lauryl sulfate, sodium carboxymethyl cellulose).

    The drug enhances the effect of anti-inflammatory, antipyretic and analgesic drugs for local and systemic use.

    Special instructions:
    Only for dental local use.
    The absence of sugar in the composition makes it possible to use the drug in patients with diabetes mellitus.
    Do not use the drug in the presence of allergic reactions to drugs from the group of non-steroidal anti-inflammatory drugs, local anesthetics (lidocaine) or benzalkonium chloride.
    If there is no effect from the use of the drug or if it worsens, immediately consult a doctor.
    In case of accidental ingestion, seek medical attention.
    Form release / dosage:Dental gel.
    Packaging:For 10 grams of gel in a tube of laminated aluminum, 1 tube in a cardboard box with instructions for use.
    Storage conditions:Store at a temperature not exceeding 25 ° C. Do not freeze.
    Shelf life:
    2 years.
    Do not use after the expiry date printed on the package.
    Terms of leave from pharmacies:Without recipe
    Registration number:LSR-009306/09
    Date of registration:18.11.2009 / 28.02.2013
    The owner of the registration certificate:Dr. Reddy's Laboratories Ltd.Dr. Reddy's Laboratories Ltd. India
    Manufacturer: & nbsp
    Representation: & nbspDR REDDY'S LABORATORIS LTD. DR REDDY'S LABORATORIS LTD. India
    Information update date: & nbsp11.03.2016
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