Belosalic

Poland
Brand name Belosalic
Form ointment
Active substance / Dosage
Betamethasone · 0.5 mg/g
Salicylic acid · 30 mg/g
Prescription type Prescription only
ATC code
Registration number 100363870
Manufacturer Belupo s.r.o.
Belosalic ointment

Package leaflet: Information for the user

Warning! Keep this leaflet! Information on the immediate packaging is in a foreign language.
Belosalic
(0.5 mg + 30 mg)/g, ointment
Betamethasone + Salicylic acid
Please read the entire leaflet carefully before using the medicine, as it contains
important information for the patient.

  • Keep this leaflet to be able to read it again if necessary.
  • If you have any doubts, consult your doctor or pharmacist.
  • This medicine has been prescribed strictly for a specific individual. Do not pass it on to others. The medicine may harm another person, even if their symptoms are identical.
  • If the patient experiences any adverse reactions, including any not listed in this leaflet, inform the doctor or pharmacist. See section 4.

Table of contents of the leaflet

  1. What Belosalic is and what it is used for
  2. Important information before using Belosalic
  3. How to use Belosalic
  4. Possible side effects
  5. How to store Belosalic
  6. Contents of the pack and other information

1. What Belosalic is and what it is used for

Belosalic ointment contains the active substances: betamethasone (in the form of betamethasone dipropionate) and salicylic acid.
Betamethasone dipropionate is a synthetic fluorinated corticosteroid for topical use in dermatology, which exerts a strong anti-inflammatory, antipruritic, and vasoconstrictive effect.
Salicylic acid exerts a keratolytic action, causing desquamation and facilitating penetration of the corticosteroid into the skin.
Indications
Belosalic ointment is indicated for local treatment of skin diseases characterized by excessive keratosis, dryness, and inflammation, which respond to topical corticosteroid therapy.

2. Important information before using Belosalic

When not to use Belosalic:

  • if the patient is allergic to the active substances or to any of the other ingredients of this medicine (listed in section 6),
  • in cutaneous tuberculosis,
  • in viral skin infections (e.g. herpes simplex, cowpox, varicella),
  • in acne, perioral dermatitis, rosacea,
  • in the anal and genital areas,
  • in diaper dermatitis,
  • in fungal or bacterial skin infections, unless appropriate causal treatment has been initiated.

Warnings and precautions
Before starting to use Belosalic, consult your doctor or pharmacist.
Do not use Belosalic ointment on hairy scalp skin.
If a skin allergic reaction (itching, burning, or redness) occurs after applying Belosalic ointment, inform your doctor. The doctor will decide whether the medicine should be discontinued immediately.
Do not use occlusive dressings or bandages, as they may enhance absorption of the medicine through the skin.
Avoid contact of the medicine with eyes and mucous membranes. Do not apply the medicine to the eyes or around the eyes.
If the patient experiences blurred vision or other visual disturbances, contact a doctor.
Use on facial skin is not recommended due to the risk of dermatitis (similar to acneiform eruptions), perioral dermatitis, skin atrophy, and acne.
In case of skin infection, the doctor will initiate appropriate antibacterial or antifungal treatment.
Since corticosteroids and salicylic acid can be absorbed through the skin, there is a risk of systemic adverse effects from corticosteroids (including suppression of adrenal cortex function) and from salicylic acid during treatment with Belosalic ointment. Therefore, avoid using the medicine over large body surface areas, on damaged skin, in high doses, for prolonged periods, and in patients with hepatic impairment or in children.
Apply Belosalic ointment to the axillae and groin areas only when absolutely necessary due to increased absorption.
Particular caution is required when using Belosalic ointment in patients with psoriasis, as topical use of corticosteroids in psoriasis may be hazardous, including the risk of disease rebound due to tolerance development, generalized pustular psoriasis, and systemic toxic effects caused by impaired skin barrier function.

Children
Use in children under 12 years of age is not recommended due to the risk of hypothalamic-pituitary-adrenal (HPA) axis suppression, Cushing's syndrome, and increased intracranial pressure following topical application of potent corticosteroids.

Belosalic and other medicines
Inform your doctor or pharmacist about any medicines the patient is currently taking, has recently taken, or might take in the future.
No interactions with other topically applied medicines are known.
Concurrent topical use of cosmetic or dermatological products used in acne treatment, products containing keratolytic agents or ethanol, and drying soaps may increase skin irritation.

Pregnancy, breastfeeding, and fertility
If the patient is pregnant or breastfeeding, suspects she may be pregnant, or is planning to have a baby, she should consult a doctor or pharmacist before using this medicine.

Pregnancy
Use of Belosalic ointment in pregnant women is permitted only if the doctor considers that the benefit to the pregnant woman outweighs the risk to the fetus. However, such use should be short-term and limited to small body surface areas.
There are no data or only limited data on the use of betamethasone dipropionate and salicylic acid in pregnant women. However, it is known that these substances may be absorbed through the skin.

Breastfeeding
The doctor will consider whether to discontinue breastfeeding or to discontinue treatment with Belosalic ointment, taking into account the benefits of breastfeeding for the child and the benefits of treatment for the mother.
Do not apply the medicine to the skin of the breasts before breastfeeding.
It is not known whether topically applied corticosteroids, including betamethasone dipropionate, are absorbed through the skin to such an extent that they can pass into breast milk. Systemic corticosteroids are known to pass into breast milk.
Salicylic acid may be absorbed into the body after application to the skin.

Driving and operating machinery
Belosalic ointment has no influence on the ability to drive or operate machinery.

3. How to use Belosalic

This medicine should always be used as directed by the physician. In case of doubt, consult a
physician or pharmacist.
Belosalic ointment is intended for topical use only.
Adults and children over 12 years of age
A thin layer of the medicine should be gently rubbed into the affected areas of the skin, usually
twice daily. In milder cases, less frequent application may be sufficient.
Do not use for longer than 14 days.
Use in children
Use of this medicine is not recommended in children under 12 years of age.
Use of a higher than recommended dose of Belosalic
Prolonged use (more than 2 weeks), application over large skin areas or damaged skin, use under
occlusive dressings, and use in children may lead to increased systemic absorption of the active
substances, resulting in overdose and general adverse effects of corticosteroids and salicylic acid.
Symptoms of corticosteroid overdose include, among others: suppression of the hypothalamic– pituitary–adrenal axis, Cushing's syndrome, benign intracranial hypertension, growth and
development retardation in children, increased blood glucose levels (hyperglycemia), and
glucosuria.
Symptoms of salicylic acid overdose include, among others: pallor, fatigue, drowsiness,
hyperventilation with rapid breathing, nausea, vomiting, hearing disturbances, and disorientation.
In case of application of a higher than recommended dose, seek immediate medical advice.
The physician will decide whether to discontinue the medicine.
If symptoms such as fever, muscle pain, joint pain, and general weakness occur, the physician may
consider administering a systemic corticosteroid.
Missed dose of Belosalic
Do not apply a double dose to make up for a missed dose.
Discontinuation of Belosalic
If you have any further questions regarding the use of this medicine, consult your
physician or pharmacist.

4. Possible adverse effects

Like all medicines, this medicine can cause adverse effects, although not everyone will experience them.
Local application of betamethasone dipropionate may cause atrophic skin changes,
irreversible striae, dry skin, dilation of small arteries, folliculitis,
hypertrichosis, acne-like changes, allergic contact dermatitis (burning, swelling, and inflammatory blisters on the skin), perioral dermatitis, itching, skin discoloration, suppression of sweat gland function (miliaria), and secondary infections.
Local application of salicylic acid may cause skin inflammation.
Systemic absorption of the active substances into the bloodstream may also lead to general adverse effects of betamethasone and salicylic acid (see above – Use of a higher than recommended dose of Belosalic).
General adverse effects are rare (occurring in 1 to 10 patients per 10,000), primarily in cases of prolonged use, application over a large skin surface area, use under occlusive dressing, and use in children, and usually resolve after discontinuation of the medicine.
Frequency unknown (cannot be estimated from available data): blurred vision.
Reporting of adverse effects
If any adverse effects occur, including any adverse effects not listed in this leaflet, inform your doctor or pharmacist. Adverse effects can be reported directly to the Department of Monitoring Adverse Drug Reactions of the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products, Al. Jerozolimskie 181C, 02-222 Warsaw, tel.: + 48 22 49 21 301, fax: + 48 22 49 21 309, website: https://smz.ezdrowie.gov.pl.
Reporting adverse effects helps to obtain more information on the safety of the medicine.

5. How to store Belosalic

Keep this medicine out of sight and reach of children.
Store below 25°C. Do not freeze.
Shelf life after first opening of the tube: 12 months.
Do not use this medicine after the expiry date stated on the packaging. The expiry date refers to the last day of the stated month.
Medicines must not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. Such measures help protect the environment.

6. Contents of the packaging and other information

What Belosalic contains

  • The active substances are (in 1 g of ointment): 0.5 mg betamethasone (as betamethasone dipropionate 0.64 mg) and 30 mg salicylic acid.
  • Other ingredients are: liquid paraffin and white soft paraffin.

What Belosalic looks like and contents of the pack
Belosalic is an ointment.
The available pack consists of a tube containing 30 g of ointment, placed in a cardboard box.
For further information, please contact the responsible party or the parallel importer.
Responsible party in the Czech Republic, country of export:
Belupo s.r.o.
Cukrová 14
811 08 Bratislava
Slovak Republic
Manufacturer:
Belupo lijekovi i kozmetika, d.d.
Ulica Danica 5
48 000 Koprivnica
Republic of Croatia
Parallel importer:
InPharm Sp. z o.o.
ul. Strumykowa 28/11
03-138 Warsaw
Repackaged in:
InPharm Sp. z o.o. Services sp. k.
ul. Chełmżyńska 249
04-458 Warsaw
Marketing authorisation number in the Czech Republic, country of export: 46/023/82-S/C
Parallel import authorisation number: 75/16