Beloderm cream d / outside. approx. 0.05% 40g
Dosage:
0.05% x 15g
0.05% x 30g
0.05% x 40g
0.05% + 0.1% x 30g
0.05% + 0.1% x 40g
0.05% + 0.1% x 5g
1 g of cream contains 0.64 mg betamethasone dipropionate (corresponding to 0.5 mg betamethasone), gentamicin sulfate (based on base) 1 mg
Release form:
Cream
Ointment
Category
Psoriasis
Scope of the drug
Leather
Release form
Cream
Manufacturer country
Croatia
Package quantity, pcs
one
Release form
Ointment for external use 0.05%.
Packaging
Tuba 30 g.
pharmachologic effect
GCS for external use.
It has anti-inflammatory, antipruritic, antiallergic, vasoconstrictor, antiexudative and antiproliferative effects.
When applied to the surface of the skin, the drug has a quick and strong effect in the focus of inflammation, reducing the severity of objective symptoms (erythema, edema, lichenification) and subjective sensations (itching, irritation, pain).
Indications
Conditions in which therapy with topical corticosteroids is effective, including:
- Atopic dermatitis.
- Neurodermatitis.
- Allergic contact dermatitis.
- Eczema (various forms).
- Contact dermatitis (including professional).
- Non-allergic dermatitis (including solar and radiation dermatitis).
- Reactions to insect bites.
- Psoriasis.
- Bullous dermatoses.
- Discoid lupus erythematosus.
- Lichen planus.
- Exudative erythema multiforme.
- Skin itching of various etiologies.
Contraindications
- Tuberculosis of the skin.
- Cutaneous manifestations of syphilis.
- Chickenpox.
- Viral, bacterial and fungal skin infections.
- Skin post-vaccination reactions.
- Open wounds.
- Trophic ulcers.
- Rosacea.
- Acne vulgaris.
- Tumors of the skin and subcutaneous structures.
- Children up to age 6 months.
- Hypersensitivity to betamethasone or to any of the auxiliary components of the drug.
Application during pregnancy and lactation
The use of the drug Beloderm in pregnant women is allowed in cases where the intended benefit to the mother outweighs the risk to the fetus.
In such cases, the use of the drug should be short-lived and limited to small areas of the skin.
During the period of breastfeeding, the use of the drug is possible according to strict indications, but the drug should not be applied to the skin of the breast before feeding.
special instructions
Long-term use of the drug on the skin of the face is not recommended.
development of rosacea, perioral dermatitis and acne is possible.
The drug should not be used in the eye area, due to the likelihood of getting the drug on the mucous membrane, which can contribute to the development of cataracts, glaucoma, fungal infections of the eye and exacerbation of herpes infection.
Some areas of the body, such as the armpits, inguinal folds, where natural occlusion exists, are more at risk of developing stretch marks, so the use of the drug on these areas of the skin should be short-lived.
With the development of a fungal or bacterial infection on the skin, additional use of an antibacterial or antifungal agent is necessary.
Use in pediatrics
The drug can be administered to children from 6 months of age with caution and for the shortest possible time.
Do not use the drug under bandages and, especially under plasticized diapers, because
this enhances the absorption of the drug and increases the risk of side effects.
Influence on the ability to drive vehicles and use mechanisms
There are no data on the adverse effects of Beloderm on the ability to drive vehicles and mechanisms.
Structure
1 g of ointment contains:
Active substance: betamethasone dipropionate - 640 mcg, which corresponds to the content of betamethasone - 500 mcg.
Excipients: chlorocresol, sodium dihydrogen phosphate monohydrate, phosphoric acid, petrolatum, mineral oil, macrogol cetostearate, cetostearyl alcohol (60% cetyl alcohol, 40% stearyl alcohol), sodium hydroxide, water.
Method of administration and dosage
The drug is intended for external use only.
Topical cream or ointment
Name ENG
BELOGENT
Clinical and pharmacological group
Drug with antibacterial and anti-inflammatory action for external use
ATX code
Betamethasone in combination with antibiotics
Dosage
0.05% x 30g
Structure
1 g of ointment contains: Active substance: betamethasone dipropionate - 640 Ојg, which corresponds to the content of betamethasone - 500 Ојg.
Excipients: mineral oil, petroleum jelly.
Indications
Conditions in which therapy with topical corticosteroids is effective, including:
Atopic dermatitis.
Neurodermatitis.
Allergic contact dermatitis.
Eczema (various forms).
Contact dermatitis (including professional).
Non-allergic dermatitis (including solar and radiation dermatitis).
Reactions to insect bites.
Psoriasis.
Bullous dermatoses.
Discoid lupus erythematosus.
Lichen planus.
Exudative erythema multiforme.
Itching of various etiologies.
Storage conditions and periods
At a temperature not higher than 25 degrees.
Expiration date: 5 years
Contraindications
Lupus.
Cutaneous manifestations of syphilis.
Chickenpox.
Viral, bacterial and fungal skin infections.
Post-vaccination skin reactions.
Open wounds.
Trophic ulcers.
Rosacea.
Acne vulgaris.
Tumors of the skin and subcutaneous structures.
Children up to age 6 months
Hypersensitivity to betamethasone or to any of the auxiliary components of the drug.
INN / Active ingredient
betamethasone, gentamicin (sulfate form)
Specifications
Category
Psoriasis
Scope of the drug
Leather
Release form
Ointment
Manufacturer country
Croatia
Package quantity, pcs
one
Minimum age from
1 year
Way of introduction
Locally
,
On the skin
,
Outwardly
Vacation conditions
Without recipe
Brand name
Belupo
The amount of the dosage form in the primary package
30 g
Primary packaging type
Tuba
Type of consumer packaging
Pack of cardboard
Pharmaco-therapeutic group
Topical glucocorticosteroid
Anatomical and therapeutic characteristics
D07AC01 Betamethasone
Dosage form
Ointment for external use
Expiration date in days
1826
The target audience
Children
Package weight, g
25
Mode of application
: https://translate.google.com/translate?hl=&sl=ru&tl=en&u=https://zz.buy-pharm.com/xzzakco.html;Description
Release form
Cream for external use 0.05%.
Packaging
Tube 40 g.
pharmachologic effect
GCS for external use.
It has anti-inflammatory, antipruritic, antiallergic, vasoconstrictor, antiexudative and antiproliferative effects.
When applied to the surface of the skin, the drug has a quick and strong effect in the focus of inflammation, reducing the severity of objective symptoms (erythema, edema, lichenification) and subjective sensations (itching, irritation, pain).
Indications
Conditions in which therapy with topical corticosteroids is effective, including:
- Atopic dermatitis.
- Neurodermatitis.
- Allergic contact dermatitis.
- Eczema (various forms).
- Contact dermatitis (including professional).
- Non-allergic dermatitis (including solar and radiation dermatitis).
- Reactions to insect bites.
- Psoriasis.
- Bullous dermatoses.
- Discoid lupus erythematosus.
- Lichen planus.
- Exudative erythema multiforme.
- Skin itching of various etiologies.
Contraindications
- Tuberculosis of the skin.
- Cutaneous manifestations of syphilis.
- Chickenpox.
- Viral, bacterial and fungal skin infections.
- Skin post-vaccination reactions.
- Open wounds.
- Trophic ulcers.
- Rosacea.
- Acne vulgaris.
- Tumors of the skin and subcutaneous structures.
- Children up to age 6 months.
- Hypersensitivity to betamethasone or to any of the auxiliary components of the drug.
Application during pregnancy and lactation
The use of the drug Beloderm in pregnant women is allowed in cases where the intended benefit to the mother outweighs the risk to the fetus.
In such cases, the use of the drug should be short-lived and limited to small areas of the skin.
During the period of breastfeeding, the use of the drug is possible according to strict indications, but the drug should not be applied to the skin of the breast before feeding.
special instructions
Long-term use of the drug on the skin of the face is not recommended.
development of rosacea, perioral dermatitis and acne is possible.
The drug should not be used in the eye area, due to the likelihood of getting the drug on the mucous membrane, which can contribute to the development of cataracts, glaucoma, fungal infections of the eye and exacerbation of herpes infection.
Some areas of the body, such as the armpits, inguinal folds, where natural occlusion exists, are more at risk of developing stretch marks, so the use of the drug on these areas of the skin should be short-lived.
With the development of a fungal or bacterial infection on the skin, additional use of an antibacterial or antifungal agent is necessary.
Use in pediatrics
The drug can be administered to children from 6 months of age with caution and for the shortest possible time.
Do not use the drug under bandages and, especially under plasticized diapers, because
this enhances the absorption of the drug and increases the risk of side effects.
Influence on the ability to drive vehicles and use mechanisms
There are no data on the adverse effects of Beloderm on the ability to drive vehicles and mechanisms.
Structure
1 g of cream contains:
Active substance: betamethasone dipropionate - 640 mcg, which corresponds to the content of betamethasone - 500 mcg.
Excipients: chlorocresol, sodium dihydrogen phosphate monohydrate, phosphoric acid, petrolatum, mineral oil, macrogol cetostearate, cetostearyl alcohol (60% cetyl alcohol, 40% stearyl alcohol), sodium hydroxide, water.
Method of administration and dosage
The drug is intended for external use only.
Topical cream or ointment
Name ENG
BELOGENT
Clinical and pharmacological group
Drug with antibacterial and anti-inflammatory action for external use
ATX code
Betamethasone in combination with antibiotics
Dosage
0.05% x 40g
Structure
1 g of cream contains:.
Active substance: betamethasone dipropionate - 640 mcg, which corresponds to the content of betamethasone - 500 mcg.
...
Excipients: chlorocresol, sodium dihydrogen phosphate monohydrate, phosphoric acid, petrolatum, mineral oil, macrogol cetostearate, cetostearyl alcohol (60% cetyl alcohol, 40% stearyl alcohol), sodium hydroxide, water.
INN / Active ingredient
betamethasone, gentamicin (sulfate form)
Storage conditions and periods
At a temperature not higher than 25 degrees.
Expiration date: 5 years
Specifications
Category
Psoriasis
Scope of the drug
Leather
Release form
Cream
Manufacturer country
Croatia
Package quantity, pcs
one
Minimum age from
1 year
Way of introduction
Locally
,
On the skin
,
Outwardly
Vacation conditions
Without recipe
Brand name
Belupo
The amount of the dosage form in the primary package
40 g
Primary packaging type
Tuba
Type of consumer packaging
Pack of cardboard
Pharmaco-therapeutic group
Topical glucocorticosteroid
Anatomical and therapeutic characteristics
D07AC01 Betamethasone
Dosage form
Cream for external use
The target audience
Children
Expiration date in days
1826
Package weight, g
55
Mode of application
:
The drug is intended for external use only. < br> Cream or ointment for external use is applied to the affected area of ​​the skin with a thin layer 2 times / day, gently rubbing. For areas with denser skin (for example, elbows, palms and feet), or where the product is easy to wear off, the product can be applied more frequently. The duration of continuous treatment is usually no more than 4 weeks. < br> < br> To prevent relapses in the treatment of chronic diseases, therapy should be continued for some time after the disappearance of all symptoms. < br> < br> Repeated courses of therapy are possible during the year. < br> < br> Cream for external use is used for the treatment of acute, incl. weeping skin lesions.
Information on technical characteristics, delivery set, country of manufacture "