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Sinaflan (Ointment, Liniment) Instructions for Use

ATC Code

D07AC04 (Fluocinolone acetonide)

Active Substance

Fluocinolone acetonide (Rec.INN registered by WHO)

Clinical-Pharmacological Group

Topical corticosteroids for external use

Pharmacotherapeutic Group

Corticosteroids used in dermatology; corticosteroids; high-potency corticosteroids (group III)

Pharmacological Action

Topical glucocorticosteroid; inhibits the release of inflammatory mediators. When applied to the skin, it prevents the marginal accumulation of neutrophils, leading to a reduction in inflammatory exudate and cytokine production; inhibits macrophage migration, and reduces infiltration and granulation processes.

It has anti-inflammatory, anti-allergic, anti-exudative, and antipruritic effects. It reduces or eliminates inflammatory skin reactions.

Pharmacokinetics

Fluocinolone acetonide easily penetrates the stratum corneum of the epidermis upon topical application, is not subject to biotransformation, and accumulates.

Absorption of fluocinolone is enhanced when applied to thin skin in the fold areas or on the face, as well as on areas with damaged epidermis or skin affected by an inflammatory process.

When using an occlusive dressing, frequent application, or application to a large skin surface, the percutaneous absorption of fluocinolone increases. In children, the absorption of fluocinolone through the skin is more pronounced than in adults.

It is metabolized in the liver to form inactive metabolites. It is excreted by the kidneys and, to a lesser extent, through the intestines with bile, mainly in the form of compounds with glucuronic acid, and also in small amounts unchanged.

Indications

Acute and chronic inflammatory and allergic skin diseases of non-microbial etiology sensitive to glucocorticosteroids, including seborrheic dermatitis, atopic dermatitis, eczema of various origins and locations, skin itching, psoriasis; sunburns; insect bites.

ICD codes

ICD-10 code Indication
L20.8 Other atopic dermatitis (neurodermatitis, eczema)
L21 Seborrheic dermatitis
L23 Allergic contact dermatitis
L24 Irritant contact dermatitis
L28.0 Lichen simplex chronicus (circumscribed neurodermatitis)
L29 Pruritus
L30.0 Nummular eczema
L40 Psoriasis
L50 Urticaria
L55 Sunburn
T14.0 Superficial injury of unspecified body region (including abrasion, bruise, contusion, hematoma, bite of nonvenomous insect)
ICD-11 code Indication
9A06.70 Atopic eczema of the eyelids
EA80.0 Infantile atopic eczema
EA80.1 Childhood atopic eczema
EA80.2 Adult atopic eczema
EA80.Z Atopic eczema, unspecified
EA81.Z Seborrheic dermatitis, unspecified
EA82 Nummular dermatitis
EA83.00 Lichen simplex of vulva
EA83.01 Lichen simplex of male genital organs
EA83.02 Lichen simplex of perianal area
EA83.0Z Lichen simplex of unspecified location
EA85.20 Atopic hand eczema
EA90.Z Psoriasis, unspecified
EC90.Z Itching, unspecified
EH92 Dermatoses provoked by friction or mechanical impact
EH92.1 Blister due to friction
EK00.Z Allergic contact dermatitis, unspecified
EK02.Z Irritant contact dermatitis, unspecified
ND56.0 Superficial injury of unspecified body region

Dosage Regimen

The method of application and dosage regimen for a specific drug depend on its form of release and other factors. The optimal dosage regimen is determined by the doctor. It is necessary to strictly adhere to the compliance of the dosage form of a specific drug with the indications for use and dosage regimen.

Ointment

Adults and children over 2 years externally.

Apply a small amount of the preparation to the skin, previously wiped with a swab moistened with an antiseptic liquid, 2-4 times a day and rub in gently. The duration of treatment depends on the nature of the disease and is usually 5-10 days, for long-term diseases up to 25 days.

For limited lesions, to enhance the effect, the ointment can be applied under an occlusive dressing. Do not apply more than 2 g of ointment per day under a dressing. The ointment is preferably used for dry forms of dermatoses.

Liniment

Apply externally 1-3 times/day, depending on the patient’s age and the dosage form used. The duration of treatment depends on the nature of the disease and the effectiveness of therapy.

Adverse Reactions

Possibleburning, skin itching, dry skin, steroid acne, folliculitis; development of secondary infectious skin lesions and atrophic changes in it.

With long-term use — secondary immunodeficiency, hypertrichosis, alopecia, especially in women, skin atrophy, hirsutism, telangiectasias, purpura, pigmentation disorder.

When applied to extensive surfaces, systemic manifestations are possible ( gastritis, steroid gastric ulcer, adrenal insufficiency, Cushing’s syndrome, steroid diabetes, striae, slowing of reparative processes); with topical use of glucocorticosteroids, systemic reactions such as blurred vision have been noted. When applied to the skin of the eyelids, the development of glaucoma or cataract is possible; rarely – central serous chorioretinopathy.

Contraindications

Hypersensitivity to fluocinolone acetonide or other glucocorticosteroids; bacterial, fungal and viral infections, skin manifestations of syphilis, acne, rosacea, perioral dermatitis, anogenital itching, skin tuberculosis, skin cancer, burns, wounds, trophic leg ulcers; post-vaccination reactions; pregnancy, breastfeeding period; children under 2 years of age.

With caution

Application to large areas of skin, damaged skin, use of large doses, long-term therapy (especially in children over 2 years); application to the skin of the face, areas with thin skin and intertriginous skin (skin folds, armpits, groin area, bends of arms and legs); application to the skin around the eyes or eyelids (risk of developing glaucoma, cataract), including in patients with glaucoma or cataract. Atrophic changes in the subcutaneous tissue, especially in the elderly. Use in girls during puberty.

Use in Pregnancy and Lactation

Contraindicated for use during pregnancy and lactation (breastfeeding). If use during lactation is necessary, the issue of discontinuing breastfeeding should be decided. It is not recommended to apply the product to the skin of the mammary glands.

Pediatric Use

Contraindicated for use in children under 2 years of age. In children over 2 years of age, it should be used with caution, under medical supervision, with minimal effective doses, on small areas of skin, in short courses (no more than 5 days); should not be applied to the skin of the face. Should be used with caution in girls during puberty.

Geriatric Use

Should be prescribed with caution to elderly patients due to atrophic changes in the subcutaneous tissue in this category of patients.

Special Precautions

Fluocinolone acetonide is recommended to be used in short courses on small areas of skin. With long-term use and/or application to large skin surfaces, damaged skin, when using large doses, when using occlusive dressings, and during therapy in children, systemic absorption of fluocinolone acetonide is possible; suppression of the hypothalamic-pituitary-adrenal system function and the development of symptoms of hypercortisolism are possible.

On the skin of the face, more often than on other body surfaces, atrophic changes may appear after prolonged topical use of glucocorticosteroids.

With long-term glucocorticosteroid therapy, sudden discontinuation of therapy may lead to the development of a “rebound syndrome”, manifested in the form of dermatitis with intense skin redness and a burning sensation. Therefore, after long-term treatment, discontinuation of fluocinolone acetonide should be carried out gradually, for example, by switching to an intermittent treatment regimen before completely stopping it.

During therapy with fluocinolone acetonide, periodic monitoring of adrenal cortex function is necessary, with determination of cortisol levels in blood and urine after adrenal stimulation with ACTH.

In patients with common or rosacea on the background of fluocinolone acetonide therapy, exacerbation of the disease is possible. To prevent local infectious complications, it is recommended to prescribe in combination with antimicrobial agents.

If during the use of fluocinolone acetonide the patient experiences symptoms such as blurred vision or other visual disturbances, consultation with an ophthalmologist is recommended to determine the possible causes of the disorders, which may include cataract, glaucoma, or rare diseases such as central serous chorioretinopathy.

Fluocinolone acetonide should be used with particular caution in patients with psoriasis due to the possible relapse of the disease caused by the development of tolerance, the risk of generalized pustular psoriasis, and general toxicity due to pressure sores.

Fluocinolone acetonide is compatible with antimicrobial agents.

Use in pediatrics

Fluocinolone acetonide can be used in children over 2 years of age. It must be taken into account that in young children, skin folds, diapers, and nappies can have an effect similar to that of an occlusive dressing and increase the systemic absorption of fluocinolone acetonide. Furthermore, in children, a greater degree of systemic absorption is possible due to the ratio between body surface area and body weight, as well as due to insufficient skin maturity. Long-term use of glucocorticosteroids in children can lead to disturbances in their growth and development. Fluocinolone acetonide is used with caution in girls during puberty.

Long-term use of fluocinolone acetonide in children is possible only under medical supervision, in the minimum dose sufficient to achieve the effect. In children, the course of treatment should not exceed 5 days.

Drug Interactions

With simultaneous use, Fluocinolone acetonide reduces the activity of antihypertensive, diuretic, antiarrhythmic medicinal products, potassium preparations.

With simultaneous use of diuretics (except potassium-sparing ones), the risk of hypokalemia increases.

During treatment with glucocorticosteroids, vaccination and immunization should not be carried out, due to the immunosuppressive effect of these agents. Fluocinolone acetonide may enhance the effect of immunosuppressive drugs and weaken the effect of immunostimulating drugs.

Storage Conditions

Store at 2°C (36°F) to 25°C (77°F). Keep in original packaging, protected from light. Keep out of reach of children.

Dispensing Status

Over-the-Counter

Important Safety Information

This information is for educational purposes only and does not replace professional medical advice. Always consult your doctor before use. Dosage and side effects may vary. Use only as prescribed.

Medical Disclaimer

Brand (or Active Substance), Marketing Authorisation Holder, Dosage Form

Marketing Authorization Holder

Altayvitamins, JSC (Russia)

Dosage Form

Bottle OTC Icon Sinaflan Ointment for external use 0.025%: 10 g or 15 g tubes

Dosage Form, Packaging, and Composition

Ointment for external use 0.025% from light yellow to yellow in color.

1 g
Fluocinolone acetonide 250 mcg

Excipients: propylene glycol, medical vaseline, anhydrous lanolin, ceresin.

10 g – aluminum tubes (1) – cardboard packs.
15 g – aluminum tubes (1) – cardboard packs.

Marketing Authorization Holder

Atoll LLC (Russia)

Manufactured By

Ozon, LLC (Russia)

Dosage Form

Bottle OTC Icon Sinaflan Ointment for external use 0.025%: 10 g or 15 g tubes

Dosage Form, Packaging, and Composition

Ointment for external use from light yellow to yellow in color, with a characteristic odor.

100 g
Fluocinolone acetonide 0.025 g

Excipients: vaseline – 80 g, ceresin – 10 g, lanolin – 5 g, propylene glycol – 4.975 g.

10 g – aluminum tubes (1) – cardboard packs.
15 g – aluminum tubes (1) – cardboard packs.

Marketing Authorization Holder

Zelenaya Dubrava, CJSC (Russia)

Dosage Form

Bottle OTC Icon Sinaflan Ointment for external use 0.025%: tubes 10 g, 15 g or 20 g

Dosage Form, Packaging, and Composition

Ointment for external use from yellowish-white to yellow in color, homogeneous, with a characteristic odor.

100 g
Fluocinolone acetonide (Sinaflan) 0.025 g

Excipients: propylene glycol – 4.975 g, lanolin (anhydrous lanolin) – 5 g, ceresin – 5 g, vaseline (medical vaseline) – 85 g.

10 g – aluminum tubes (1) – cardboard packs.
15 g – aluminum tubes (1) – cardboard packs.
20 g – aluminum tubes (1) – cardboard packs.
10 g – tubes made of combined material (1) – cardboard packs.
15 g – tubes made of combined material (1) – cardboard packs.
20 g – tubes made of combined material (1) – cardboard packs.

Marketing Authorization Holder

Murom Instrument-Making Plant, JSC (Russia)

Dosage Form

Bottle OTC Icon Sinaflan Ointment for external use 0.025%: 10 g or 15 g tubes

Dosage Form, Packaging, and Composition

Ointment for external use from light yellow to yellow in color, homogeneous.

100 g
Fluocinolone acetonide 0.025 g

Excipients: propylene glycol, vaseline, anhydrous lanolin, ceresin.

10 g – aluminum tubes (1) – cardboard packs.
15 g – aluminum tubes (1) – cardboard packs.

Marketing Authorization Holder

Murom Instrument-Making Plant, JSC (Russia)

Dosage Form

Bottle OTC Icon Sinaflan Liniment for external use 0.025%: 15 g tube

Dosage Form, Packaging, and Composition

Liniment for external use yellowish-white in color.

100 g
Fluocinolone acetonide 0.025 g

Excipients: propylene glycol, vaseline, anhydrous lanolin, pentaerythrityl dioleate, stearic acid, methylparaben, propylparaben, purified water.

15 g – aluminum tubes (1) – cardboard packs.

Marketing Authorization Holder

Nizhpharm JSC (Russia)

Dosage Form

Bottle OTC Icon Sinaflan Ointment for external use 0.025%: 10 g or 15 g tubes

Dosage Form, Packaging, and Composition

Ointment for external use from light yellow to yellow in color.

1 g
Fluocinolone acetonide (Sinaflan) 0.25 mg

Excipients: citric acid monohydrate, propylene glycol, ceresin, lanolin, vaseline.

10 g – aluminum tubes (1) – cardboard packs.
15 g – aluminum tubes (1) – cardboard packs.

Marketing Authorization Holder

Promomed Rus LLC (Russia)

Manufactured By

Biokhimik, JSC (Russia)

Dosage Form

Bottle Rx Icon Sinaflan Ointment for external use 0.025%: 15 g tube

Dosage Form, Packaging, and Composition

Ointment for external use is homogeneous, ranging from light yellow to yellow in color, with a characteristic odor.

100 g
Fluocinolone acetonide 0.025 g

Excipients: propylene glycol – 4.975 g, petrolatum – 80 g, anhydrous lanolin – 5 g, ceresin – 10 g.

15 g – aluminum tubes (1) with caps – cardboard packs.

Marketing Authorization Holder

Tula Pharmaceutical Factory, LLC (Russia)

Dosage Form

Bottle OTC Icon Sinaflan Ointment for external use 0.025%: 10 g or 15 g tubes

Dosage Form, Packaging, and Composition

Ointment for external use ranges from light yellow to yellow in color.

100 g
Fluocinolone acetonide 0.025 g

Excipients: 1,2-propylene glycol, medical petrolatum, anhydrous lanolin, ceresin.

10 g – aluminum tubes (1) – cardboard packs.
15 g – aluminum tubes (1) – cardboard packs.

Marketing Authorization Holder

Altayvitamins, JSC (Russia)

Dosage Form

Bottle OTC Icon Sinaflan ointment 0.025% Ointment for external use 0.025%: 10 g or 15 g tubes

Dosage Form, Packaging, and Composition

Ointment for external use 0.025% 1 g
Fluocinolone acetonide 250 mcg

Excipients: propylene glycol, medical petrolatum, anhydrous lanolin, ceresin.

15 g – aluminum tubes (1) – cardboard packs.
10 g – aluminum tubes (1) – cardboard packs.

Marketing Authorization Holder

Akrikhin Chemical and Pharmaceutical Plant, JSC (Russia)

Dosage Form

Bottle OTC Icon Sinaflan-Akrikhin Ointment for external use 0.025%: 10 g or 15 g tubes

Dosage Form, Packaging, and Composition

Ointment for external use ranges from light yellow to yellow in color.

100 g
Fluocinolone acetonide calculated as 100% substance 0.025 g

Excipients: propylene glycol – 4.975 g, petrolatum – 80 g, lanolin – 5 g, hard paraffin – 10 g.

10 g – tubes (1) – cardboard packs.
15 g – tubes (1) – cardboard packs.

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