Stomaflor® (Stomaflor)

Composition Pharmacodynamics Indications Carefully Contraindications Dosing and Administration Side effects Form release / dosage
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Dosage form: & nbspointment for topical application
Composition:

1 g of ointment contains:

active ingredients:

bifidobacteria AT. bifidum 1, sorbed on silicon dioxide colloid - not less than 5x106 CFU, lactobacilli L. plantarum 8P-A3, sorbed on silicon dioxide colloid - not less than 5x106 CFU, sea buckthorn oil concentrate - 0.06 in

Excipients:

sunflower oil - 0.036-0.044 g, polysorbate-80 0.0027 0.0033 g, polyvinylpyrrolidone low molecular weight - 0,086-0,100 g, silicon dioxide colloid - 0,00054 - 0,00066 g, Vaseline - 0.65 - 0.79 g, paraffin P2 - 0.072-0.088 g, sucrose 0.0020 0.0025 g, gelatin - 0.00027 - 0.00033 g.

Description:

Ointment is light-brown or orange, homogeneous, with a weak smell of sea-buckthorn oil.

Pharmacotherapeutic group:MIBP - eubiotic
ATX: & nbsp
  • Other preparations for topical use in diseases of the oral cavity
    • Pharmacodynamics:

    The drug Stomaflor ® has a reparative and anti-inflammatory action, restores the normal microflora of the oral cavity. The active components that make up Stomaflor ® have a complementary effect. Bifidobacteria (AT. bifidum) and lactobacilli (L.plantarum), included in the drug, suppress the growth of pathogenic and conditionally pathogenic bacteria (staphylococci, streptococci, proteus, Klebsiella, etc.), accelerate normalization of quantitative and qualitative composition of microflora: activate mucosal repair, enhance the anti-inflammatory effect of sea-buckthorn oil.

    Sea buckthorn oil is a source of carotene (provitamin A), tocopherols (vitamin E) and other lipophilic substances, reduces the intensity of free radical processes and protects cell and subcellular membranes from damage, stimulates reparative processes in mucosal lesions.

    Pharmacokinetics:

    Bifido- and lactobacilli, which are part of the drug, are not absorbed into the bloodstream. Data on the pharmacokinetics of sea buckthorn oil are absent.

    Indications:

    Gingivitis and periodontal diseases: acute and chronic gingivitis; chronic periodontitis, including chronic generalized periodontitis.

    Contraindications:Allergic reactions to sea ​​buckthorn oil.
    Pregnancy and lactation:There are no data on the use of the drug during pregnancy and breastfeeding.
    Dosing and Administration:

    In acute and chronic gingivitis (inflammation of the gums), the drug is applied to the gum area 2 times a day in the morning and in the evening, the course of treatment is 7-10 days. In the complex treatment of chronic periodontitis, including chronic generalized periodontitis,after the dentist (parodontologist) conducts the procedure for removal of dental plaque, a course of treatment with a drug that is 10-14 days is prescribed. The drug is applied by the patient to the affected surface of the gum and is introduced into the periodontal pockets 2 times a day in the morning and in the evening. The course of treatment with the drug can be repeated, the interval between courses is at least 7 days.

    In the treatment of gingivitis, the drug is applied to the affected surface of the gum after brushing the teeth. Before applying the ointment, it is necessary to dry the oral cavity with a dry cotton swab. 1 g of ointment, which corresponds to a strip of an ointment, squeezed out of a tube, 1 cm long, is applied to a clean finger, and then this finger is transferred to the focus of inflammation on the gum. With periodontal disease, the ointment is placed in the pockets of the gum. After applying the ointment, the saliva released within 5-7 minutes is swallowed, reducing its contact with the drug applied. It is not recommended to eat and drink for 30 minutes after applying the ointment, and also to remove the drug.

    Side effects:Local allergic reactions in persons with sea buckthorn intolerance.
    Overdose:

    Cases of overdose were not observed.

    Interaction:

    When taking antibiotics, the interval between taking an antibiotic and a drug Stomaflor® is recommended 3-4 hours.

    Special instructions:No.
    Effect on the ability to drive transp. cf. and fur:The drug does not affect the ability to drive vehicles, mechanisms.
    Form release / dosage:Ointment for topical application.
    Packaging:

    For 10 grams in aluminum tubes. Each tube together with the instruction for use is placed in a pack of cardboard.

    Storage conditions:

    Store at a temperature of 2 to 10 ° C.

    The opened tube should be stored at a temperature of 2 to 10 ° C for not more than 30 days.

    Keep out of the reach of children

    The drug is not suitable for use at the expiration of the expiry date, with a change in appearance, in the absence or fuzzy marking, if a breach of the integrity of the primary packaging is discovered prior to the first opening.

    Transportation conditions

    At a temperature of 2 to 10 ° C. It is allowed to transport the drug at a temperature of no higher than 25 ° C for not more than 10 days.

    Shelf life:18 months.
    Terms of leave from pharmacies:Without recipe
    Registration number:LP-004378
    Date of registration:18.07.2017
    Expiration Date:18.07.2022
    The owner of the registration certificate:PARTNER, CJSC PARTNER, CJSC Russia
    Manufacturer: & nbsp
    Information update date: & nbsp03.10.2017
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