ANGINOVAG throat spray №20ml

ANGINOVAG throat spray №20ml

Product Code: 9577
Availability: In Stock

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active substances:dequalinium chloride, tyrothricin, enoxolone (?-glycyrrhetinic acid), hydrocortisone acetate, lidocaine hydrochloride;

1 ml of spray contains dequalinium chloride 1 mg tyrothricin 4 mg enoxolone (?-glycyrrhetinate acid) 0.6 mg hydrocortisone acetate 0.6 mg lidocaine hydrochloride 1 mg

other ingredients:propylene glycol, oil of pineapple, saccharin sodium, ethanol 96% (V/V).


Dosage form

Spray for oral cavity.

basic physical and chemical properties:transparent solution, from colorless to slightly yellowish.


drug description

medicine used in diseases of the throat. Antiseptics. Code ATX R02A A20.


Pharmacological properties


Anginous combines in its composition of matter anti-inflammatory, analgesic, antibacterial and antiseptic actions, which have complementary and synergistic effect.

These pharmacological properties allow complex pathogenetic therapy of inflammatory diseases of the upper respiratory tract and mucous membranes of the oral cavity.

Pharmacokinetics.there is No systemic absorption of any active ingredients not detected.


Local treatment for infectious and inflammatory diseases of the oral cavity and upper respiratory tract: tonsillitis, pharyngitis, laryngitis, aphthous and ulcerative stomatitis, glossitis.


hypersensitivity (Allergy) to the components of the drug.


Interaction with other medicinal products and other forms of interaction

the Drug contains ethanol, it can alter or enhance the effect of other drugs.

the Antibacterial activity of dequalinium reduced while the use of anionic tenside, for example, toothpaste.

application Features

the Preparation contains ethanol. Each application includes approximately 0.075 g of ethanol, which can be a risk factor for children, breastfeeding and for patients with liver disease, alcoholism, epilepsy, brain injury or injury.

while taking the drug Anginosa possible positive doping test.

the Drug may cause skin irritation because it contains propylene glycol.

avoid getting the spray into the eyes.

use during pregnancy or lactation.Clinical data on the use of Anginous during pregnancy or lactation are not available.

Ability to influence the reaction rate when driving motor transport or operating other mechanisms.there is no evidence of harmful effects on the ability to drive and operate machinery.

Method of application and doses

for adults and children over 13 years of age. Rinse mouth and throat with boiled warm water if necessary before use. Remove necrotic plaque from affected areas (ulcers, erosion) with a tampon. The first two days - 1 to 2 sprays every 2-3 hours, followed by 1 injection every 6:00. The course of treatment is determined by the doctor individually, usually 5-7 days.

Mode of application.

for proper use, it is recommended to place the vial in an upright position so that the oral applicator is directed to the affected area, but not completely injected into the oral cavity. Press the top of the cap from top to bottom.

the Bottle is provided with a dosing valve: each press until the end causes controlled drug intake.

Children.due TO the lack of clinical data for this age group Anginosa not recommended for children under the age of 13.


Not described any cases of overdose.

Side effects

When using the drug Anginosa, in some cases, depending on the sensitivity of the patient to the drug Aginova can cause local irritation, which usually is temporary.

the following are the adverse reactions that can occur as a result of monotherapy by one of the active substances:

chloride disqualification

hypersensitivity reactions such as rash, itching, burning, irritation of the oral mucosa and throat may Sometimes occur. In rare cases, namely when the abuse, but they can cause ulcers and necrosis.


skin Irritation, allergic reactions including erythema, urticaria, contact dermatitis. There may be short-term changes in taste, temporary numbness of the tongue. Long-term use in rare cases there may be a slight coloration in yellow or light brown teeth, dental fillings and dentures, or language, you can get rid of through oral hygiene. The coloration disappears on its own after discontinuation of the drug.

acetate hydrocortisone

When applied to the skin:

on the part of the skin and subcutaneous tissue:

  • contact Allergy, pustular acne
  • The
  • skin atrophy, often irreversible, accompanied by a thinning of the epidermis, telangiectasia, purpura and striae;
  • The
  • depigmentation, hypertrichosis;
  • The
  • resizepolicy and perioral dermatitis, accompanied or not accompanied by atrophy of the skin;
  • The
  • a"rebound Effect" that can lead to steroid dependence.

Endocrine disorders:adrenocortical suppression.

Very rarely (<1/10000, including individual messages)

from the eye:increase in intraocular pressure and the risk of cataract (with systematic contact of the drug on the conjunctiva).

from the immune system:hypersensitivity reactions.

Slowing wound healing, infection, redness, irritation, burning, rash, itching, folliculitis, acne, maceration. With local use of corticosteroids, systemic adverse reactions are possible, which occur rarely, but can be serious (including Cushing's syndrome, hyperglycemia, glucosuria, growth retardation and intracranial hypertension).

lidocaine hydrochloride

local effects

when using lidocaine may experience a burning sensation, which disappears after the anesthetic effect (within 1 minute).

transient erythema, edema and decreased sensitivity may be observed at the site of application.

allergic reactions

including: skin rashes, itching, urticaria, angioedema, bronchospasm, in extremely severe cases - shock.

in case of hypersensitivity reactions, the drug should be discontinued.

System effects

the development of systemic effects is unlikely because the amount of active substance that can reach blood circulation is very small. With the use of high doses and in if rapid absorption of the lidocaine, or in case of hypersensitivity, idiosyncrasy or reduced tolerance may develop side effects such:

from the Central nervous system: excitement, depression, nervousness, dizziness, drowsiness, spasms, loss of consciousness, paralysis of respiratory organs;

on the part of the cardiovascular system:hypotension, myocardial infarction, bradycardia, cardiac arrest.


shelf Life

4 years.

storage Conditions

Store at a temperature not exceeding 30 ° C.



is Not described.



10 ml or 20 ml each in a bottle; 1 bottle each with an oral dispenser in a carton.


Category vacation

over the counter.



Ferrer Internacional, S. A.

location of the manufacturer and address of the place of business

registered Address:

Gran via Carlos III, 94, 08028, Barcelona, Spain.

Place of production:

s/Joan, Boscia, 1-9, 08173 Sant Cugat del Bayes (Barcelona), Spain.


Ameritron Extra – coated tablets. It is an anti-allergic, vasoconstrictor. It has antipyretic, analgesic effect. It is used for symptomatic therapy in infectious diseases. Part medications is acetaminophen, phenylephrine, chlorphenamine.

When should I use

the Medication is prescribed to eliminate the symptoms of colds infectious diseases:

  • Heat.
  • The
  • Aching muscles and joints.
  • The
  • Nasal respiratory tract.
  • The
  • Headache.

the Drug is not recommended for use in children under 12 years old, women during pregnancy and breastfeeding. Also, the drug is forbidden to use in a number of pathological conditions. Before use, be sure to read the annotation to the drug.

Recommendations for usage

to Apply without the control of the attending physician is allowed not more than 3 days. The drug is absorbed regardless of the consumption of food. Tablets should be washed down with warm water. 

one capsule is Prescribed every 4 hours. Daily rate-no more than 6 pieces. In the event of adverse reactions drug use should be stopped. 

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