Alorom
Ukraine
Table of Contents
INSTRUCTIONS for medical use of the medicinal product ALOROM
Composition:
Active substances: 1 g of liniment contains fresh juice of leaves of Aloe arborescens Mill. – 478 mg, liquid extract (1:1) of chamomile flowers (Matricariae flos) – 200 mg, liquid extract (1:1) of marigold (calendula) flowers (Calendulae flos) – 100 mg, levomenthol – 1 mg, eucalyptus oil – 1 mg;
Excipients: castor oil, emulsifier No. 1;
Excipients present in the composition of fresh leaf juice of Aloe arborescens: ethanol (96%), chlorobutanol, hemihydrate*; present in the composition of liquid extract (1:1) of chamomile flowers and liquid extract (1:1) of marigold (calendula) flowers: ethanol (96%), purified water.
Excipients present in the composition of emulsifier No. 1: cetyl alcohol, stearyl alcohol.
Pharmaceutical form. Liniment.
Main physicochemical properties: homogeneous thick mass, light brown to brown in color with a greenish tint, with a specific odor.
Pharmacotherapeutic group.
Medicinal products used locally for joint and muscle pain. ATC code M02AX10.
Pharmacological properties.
Pharmacodynamics.
Alorom is a combination drug that exerts anti-inflammatory and analgesic effects, improves trophic processes due to the complex action of physiologically active plant substances contained in its composition (flavonoids, tannins, anthraquinones). The drug promotes tissue repair and resorption of hematomas.
Pharmacokinetics.
Not studied.
Clinical characteristics.
Indications.
As part of complex therapy in the treatment of post-traumatic arthritis, plexitis, radiculitis, polyarthritis, myositis, tenosynovitis, external hematomas, and myalgias; for prevention of pressure ulcers.
Contraindications.
Hypersensitivity to the components of the drug, to plants of the Asteraceae (Compositae) family. Pregnancy or breastfeeding. Children under 6 years of age.
Interaction with other medicinal products and other types of interactions.
Not established.
Instructions for use.
The liniment must not be applied to open wounds or damaged skin. To enhance the therapeutic effect, it is recommended to apply dry warming dressings to the affected areas.
Use during pregnancy or breastfeeding.
The product is not recommended during pregnancy or breastfeeding.
Ability to influence reaction rate while driving or operating machinery.
Unknown.
Method of Administration and Dosage.
For topical use in adults and children aged 6 years and older. Apply a thin layer of the liniment to the skin 2–3 times daily, gently massaging the affected areas. The application area depends on the size and location of the lesion. The treatment course lasts from 5 to 15 days. If necessary, the treatment course may be repeated after 1–2 weeks following consultation with a physician.
Children.
Do not use in children under 6 years of age.
Overdose.
In case of overdose, adverse effects may be intensified.
Treatment: symptomatic therapy.
Adverse reactions.
In individual cases, allergic reactions may occur, such as skin irritation, rashes, itching, and contact dermatitis.
Shelf life. 2 years.
Storage conditions.
Store in the original packaging at a temperature between 2 °C and 8 °C.
Freezing must not be allowed.
Keep out of reach of children.
After opening the tube, the liniment may be stored throughout the course of treatment.
Packaging.
30 g in tubes, 1 tube per package.
Prescription status. Over-the-counter.
Manufacturer.
JSC "Lubnyfarm".
Manufacturer's address and place of business.
16, Barvinkova Street, Lubny, Poltava Oblast, Ukraine, 37500.
INSTRUCTION
for medical use of the medicinal product
ALOROM
Composition: Active substances: 1 g of liniment contains fresh juice of leaves of Aloe arborescens Mill. – 478 mg, liquid extract (1:1) of chamomile flowers (Matricariae flos) – 200 mg, liquid extract (1:1) of marigold (calendula) flowers (Calendulae flos) – 100 mg, levomenthol – 1 mg, eucalyptus oil – 1 mg;
Excipients: castor oil, emulsifier No. 1;
Excipients contained in fresh juice of leaves of Aloe arborescens: ethanol (96%), chlorobutanol, hemihydrate*; contained in liquid extract (1:1) of chamomile flowers and liquid extract (1:1) of marigold (calendula) flowers: ethanol (96%), purified water.
Excipients contained in emulsifier No. 1: cetyl alcohol, stearyl alcohol.
Pharmaceutical form. Liniment.
Main physicochemical properties: a homogeneous, viscous mass of light brown to brown color with a greenish tint and a characteristic odor.
Pharmatherapeutic group. Medicinal products used locally for joint and muscle pain.
ATC code M02AX10.
Pharmacological properties.
Pharmacodynamics.
Alorom is a combined preparation that exerts anti-inflammatory and analgesic effects and improves trophic processes due to the complex action of biologically active plant constituents in its composition (flavonoids, tannins, anthraquinones). The preparation promotes tissue repair and resorption of hematomas.
Pharmacokinetics.
Not studied.
Clinical characteristics.
Indications.
For use as part of complex therapy in the treatment of post-traumatic arthritis, plexitis, radiculitis, polyarthritis, myositis, tenosynovitis, external hematomas, and myalgia; for prevention of pressure ulcers.
Contraindications
Hypersensitivity to the components of the medicinal product or to plants of the Asteraceae family. Pregnancy or breastfeeding. Children under 6 years of age.
Interaction with other medicinal products and other types of interactions.
Not established.
Special precautions.
The liniment must not be applied to open wounds or damaged skin. To enhance the therapeutic effect, dry warming dressings over the affected areas are recommended.
Use during pregnancy or breastfeeding.
The medicinal product must not be used during pregnancy or breastfeeding.
Effect on the ability to drive vehicles or operate machinery. Unknown.
Method of administration and dosage.
For external use in adults and children aged 6 years and older. Apply the liniment thinly to the skin 2–3 times daily, gently massaging the affected areas. The application area depends on the size and location of the lesion. The treatment course lasts from 5 to 15 days. If necessary, the course may be repeated after 1–2 weeks following consultation with a physician.
Children.
Do not use in children under 6 years of age.
Overdose.
Overdose may lead to an increase in adverse reactions.
Treatment: symptomatic therapy.
Adverse reactions.
In individual cases, allergic reactions such as skin irritation, rashes, itching, and contact dermatitis may occur.
Shelf life. 2 years.
Storage conditions.
Store in the original packaging at a temperature between 2 °C and 8 °C.
Freezing must not be allowed.
Keep out of reach of children.
After opening the tube, the liniment may be stored throughout the course of treatment.
Packaging. 30 g in tubes, 1 tube per package.
Prescription status. Over-the-counter.
Manufacturer.
JSC "Lubnyfarm".
Manufacturer's address and place of business.
16, Barvinkova Street, Lubny, Poltava Oblast, Ukraine, 37500.