Finalgon ointment d / nar. approx. tube 20g
Release form:
Cream
Ointment
Category
Bruises, sprains
Scope of the drug
Musculoskeletal system
Release form
Ointment
Manufacturer country
Austria
Package quantity, pcs
one
Dosage form
Almost colorless or slightly brownish, transparent or translucent, homogeneous homogeneous ointment
Structure
1 g of ointment contains: nonivamide
(nonylic acid vanillilamide) (P5VA) 4 mg
nicoboxyl (nicotinic acid butoxyethyl ester) (NSBE) 25 mg
Excipients:
Diisopropyl adipate (Crodamol) 120 mg
colloidal silicon dioxide 20 mg
petroleum jelly (paraffin, soft white) 822 mg sorbic acid 2 mg, citronella oil 2 mg purified water 5 mg.
pharmachologic effect
Nonivamid
It is a synthetic analogue of capsaicin and has analgesic properties, which are manifested as a result of the gradual penetration of the substance into the peripheral nociceptive C-fibers and A-delta nerve fibers upon repeated application of the drug to the skin.
Nonivamide has a vasodilating effect, which is accompanied by an intense prolonged sensation of warmth, due to the stimulation of afferent nerve endings in the skin
Nicoboxil
It is a derivative of nicotinic acid, which has vasodilating properties with the participation of prostaglandins I2 and E2.
The hyperemic effect of nicoboxil (butoxyethyl ester of nicotinic acid) develops faster and has a greater intensity than the hyperemic effect of nonivamide.
Combined action
Nonivamide and nicoboxil have complementary vasodilating properties, cause flushing of the skin, increase the rate of enzymatic reactions, and activate metabolism.
The appearance of redness and an increase in skin temperature within a few minutes after application indicate the rapid penetration of the active components of the drug into the skin.
FINALGON's action is local.
The action of the drug develops within a few minutes.
the maximum effect occurs
after 20-30 minutes.
The analgesic effect of a combination of 0.4% nonivamide and 2.5% nicoboxil was demonstrated in a study of efficacy in patients with acute
nonspecific pain in the lower back It was found that in patients who used FINALGON (2 cm ointment per application and used the drug up to 3 times a day for 4 days), there was a clinically significant decrease in the intensity of pain in the lower back after 4 hours after the first application
On the last day of treatment, determined individually, Taske experienced a clinically significant reduction in pain.
In a clinical study, it was found that pain relief began after 1–2 hours.
Pharmacokinetics
Data on the pharmacokinetics of Finalgon® are not provided
Side effects
In the course of clinical studies and long-term experience with the drug, the following side effects were identified:
From the immune system: anaphylactic reactions, hypersensitivity.
From the nervous system: paresthesia, burning sensation
Respiratory system: cough, shortness of breath.
On the part of the skin and subcutaneous tissues: vesicles or pustules at the site of application, erythema, local skin reaction (for example, contact dermatitis), itching, rash, facial edema, urticaria, a feeling of heat at the site of application.
Selling features
Available without a prescription
Special conditions
The drug causes flushing of the skin, resulting in redness, a feeling of warmth, itching and burning at the site of application.
These symptoms may be more pronounced with excessive application of the drug or in the case of intense rubbing on the skin surface.
Using excessive amounts of the drug or vigorous rubbing on the surface of the skin may lead to the formation of vesicles or pustules at the site of application of the ointment.
After using FINALGON, wash your hands immediately with soap and water.
Care must be taken to avoid accidental contact with the drug.
Name ENG
FINALGON
Clinical and pharmacological group
A preparation with a local irritant and analgesic effect
ATX code
Other drugs
Dosage
25mg / g + 4mg / g x 20g
Structure
1 g of the ointment contains: nonivamide.
(nonylic acid vanillilamide) (P5VA) 4 mg.
nicoboxyl (nicotinic acid butoxyethyl ester) (NSBE) 25 mg.
Excipients: Diisopropyladipinate (Krodamol) 120 mg
colloidal silicon dioxide 20 mg
petroleum jelly (paraffin, soft white) 822 mg sorbic acid 2 mg, citronella oil 2 mg purified water 5 mg.
Indications
Arthritis
arthralgia and myalgia of rheumatic genesis
sports injuries, bruises and damage to the ligamentous apparatus
myalgia caused by excessive physical exertion
lumbago
neuritis
ishalgia
bursitis and tendovaginitis
for preliminary warming up" of muscles before physical exercises, sports competitions
as part of complex vasodilator therapy for peripheral circulatory disorders.
INN / Active ingredient
Nonivamide + nicoboxil
Storage conditions and periods
At a temperature not higher than 25 degrees.
Expiration date: 4 years
Contraindications
Hypersensitivity to nicoboxil, nonivamide or excipients of the drug
children under 12 years of age.
the drug should not be applied to sensitive skin, open wounds, inflamed skin areas, areas of skin with increased permeability: neck, lower abdomen, inner thighs.
Specifications
Category
Bruises, sprains
Scope of the drug
Musculoskeletal system
Release form
Ointment
Manufacturer country
Austria
Package quantity, pcs
one
Minimum age from
12 years
Way of introduction
Outwardly
Vacation conditions
Without recipe
Brand name
Boehringer ingelheim
Components
applicator
The amount of the dosage form in the primary package
20 g
Primary packaging type
Tuba
Type of consumer packaging
Pack of cardboard
Pharmaco-therapeutic group
Local irritant
Anatomical and therapeutic characteristics
M02AX10 Other preparations
Dosage form
Ointment for external use
Drug action
Analgesic
,
Pain reliever
,
Vasodilator
Dosage (volume) of the substance in the preparation
1 g - nonivamide 4 mg, nicoboxil 25 mg
The target audience
Children
Expiration date in days
1095
Package weight, g
thirty
Mode of application
:
It is necessary to start the application with the lowest dose of the drug.
To do this, using the attached applicator, a column of the drug no more than 0.5 cm in size is applied to the appropriate palm-sized area of skin with light rubbing movements.
To enhance the therapeutic effect, the area of the skin on which the drug is applied can be covered with a woolen cloth.
Information on technical characteristics, delivery set, country of manufacture "