(30 mg + 10 mg)/g, ointment
Oxytetracycline + Hydrocortisone acetate
Oxycort is an ointment.
The medicine contains the active substances: oxytetracycline and hydrocortisone acetate.
Oxytetracycline is an antibiotic from the tetracycline group, it acts on Gram-positive and Gram-negative bacteria.
Hydrocortisone acetate is a medicine from the corticosteroid group with mild anti-inflammatory action.
Applied to the skin, it acts locally anti-inflammatory, anti-itching, and vasoconstrictive.
Oxycort is used for scaly and dry changes in the following bacterial infection-complicated skin diseases:
Before starting to use Oxycort, you should discuss it with your doctor or pharmacist.
Do not use the medicine in children and adolescents.
You should tell your doctor or pharmacist about all medicines you are currently using or have recently used, as well as any medicines you plan to use.
No interactions have been found during local use of the medicine in accordance with the recommended indications and method of use.
It is not recommended to use two or more medicines locally at the same time, as this may affect the concentrations of active substances at the application site or cause skin redness.
If the patient is pregnant or breastfeeding, suspects they may be pregnant, or plans to have a child, they should consult their doctor or pharmacist before using this medicine.
The medicine should not be used during pregnancy and breastfeeding.
The effect of hydrocortisone acetate on fertility has not been studied, but other corticosteroids have been shown to affect fertility.
Oxycort does not affect the ability to drive and use machines.
This medicine should always be used in accordance with the doctor's recommendations. In case of doubts, you should consult a doctor or pharmacist.
Oxycort ointment is applied in a thin layer to the affected skin surface, no more than once or twice a day.
The ointment should not be used under an occlusive dressing (sealing).
Treatment should not be continued without interruption for more than 7 to 14 days.
On facial skin, do not use for more than 7 days.
Within one week, no more than 1 tube (10 g) of ointment can be used.
Do not use the medicine in children and adolescents.
After prolonged use on large skin surfaces, in large doses, under an occlusive dressing (sealing), or on damaged skin, the medicine may be absorbed into the blood and cause systemic corticosteroid or oxytetracycline action (see section 2: Warnings and precautions).
Do not use a double dose to make up for a missed dose. In case of any further doubts about using this medicine, you should consult a doctor, pharmacist, or nurse.
Like all medicines, Oxycort can cause side effects, although not everybody gets them.
Local side effects of unknown frequency (frequency cannot be determined from available data):
May occur: burning, itching, excessive drying, atrophic skin changes, dermatitis around the mouth, skin maceration, acne-like changes, stretch marks, diaper rash, rash, excessive hair growth, skin discoloration, secondary skin infections, and folliculitis, allergic reactions, yeast or resistant bacterial strains, blurred vision.
Prolonged use on facial skin may cause skin atrophy and vasodilation.
Irritation may occur at the site of application of the medicine.
Systemic side effects of unknown frequency (frequency cannot be determined from available data):
During prolonged use of the medicine or use on large skin surfaces, hydrocortisone acetate may be absorbed into the blood and cause systemic side effects characteristic of corticosteroids, such as adrenal gland suppression (see section 2: Warnings and precautions). These effects may occur especially if the patient uses the medicine in skin folds, groin, under an occlusive dressing (sealing), or in children.
If you experience any side effects, including any side effects not listed in this leaflet, you should consult your doctor or pharmacist.
If you experience any side effects, including any side effects not listed in this leaflet, you should tell your doctor or pharmacist. Side effects can be reported directly to the Department of Monitoring of Adverse Reactions to Medicinal Products 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 By reporting side effects, you can help gather more information on the safety of the medicine.
Do not store above 25°C.
The medicine should be stored out of sight and reach of children.
Do not use this medicine after the expiry date stated on the packaging. The expiry date refers to the last day of the specified month.
Medicines should not be disposed of via wastewater or household waste containers. You should ask your pharmacist how to dispose of medicines that are no longer used. This will help protect the environment.
Oxycort is a uniform yellow ointment.
An aluminum tube containing 10 g of ointment, in a cardboard box.
To obtain more detailed information, you should contact the marketing authorization holder or parallel importer.
Bausch Health Ireland Limited
3013 Lake Drive
Citywest Business Campus
Dublin 24, D24PPT3
Ireland
Przedsiębiorstwo Farmaceutyczne Jelfa S.A.
ul. Wincentego Pola 21
58-500 Jelenia Góra
Poland
Medezin Sp. z o.o.
ul. Zbąszyńska 3
91-342 Łódź
Medezin Sp. z o.o.
ul. Zbąszyńska 3
91-342 Łódź
CEFEA Sp. z o.o. Sp. komandytowa
ul. Działkowa 56
02-234 Warszawa
Pharma Innovations Sp. z o.o.
ul. Jagiellońska 76
03-301 Warszawa
Synoptis Industrial Sp. z o.o.
ul. Szosa Bydgoska 58
87-100 Toruń
CANPOLAND SPÓŁKA AKCYJNA
ul. Beskidzka 190
91-610 Łódź
Marketing authorization number in Lithuania, the country of export: LT/1/97/0020/001
[Information about the trademark]
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