SNUP nasal spray Stada 0.1%, 15 ml
Category
Runny nose
Scope of the medicinal product
Ear, Throat, Nose
Release form
Spray
Manufacturer country
Germany
Scope of application
Otorhinolaryngology
Colorless transparent solution.
Pharmaco-therapeutic group
N4 Acute respiratory diseases with symptoms of rhinitis (runny nose), acute allergic rhinitis, hay fever, sinusitis, eustachitis, otitis media (to reduce swelling of the nasopharyngeal mucosa), to facilitate rhinoscopy and other diagnostic procedures in the nasal passages.
Application during pregnancy and during breastfeeding
During pregnancy, the use of the drug is contraindicated.
During the period of breastfeeding, the drug should be used only after a careful assessment of the risk-benefit ratio for the mother and the infant, it is not allowed to exceed the recommended dosage.
During breastfeeding, you should consult your doctor before using Snoop®.
Dosage form
Nasal spray 0.05% and 0.1%.
15 ml nasal spray (150 doses) in a polyethylene bottle with a spray system.
1 bottle with instructions for medical use of the drug is placed in a cardboard box.
Shelf life
5 years. The contents of the bottle are sterile, without preservatives.
Do not use after the expiration date.
If a medicinal product has expired, do not throw it into wastewater or outside!
Place the medication in the trash can.
These measures will help protect the environment.
Category
Symptomatic drugs
Name ENG
SNUP
Clinical and pharmacological group
A vasoconstrictor drug for topical use in ENT practice.
ATX code
Xylometazoline
Dosage
0.1% x 15ml
Structure
1 ml of nasal spray contains: active ingredient - xylometazoline hydrochloride 0.5 mg or 1.0 mg and auxiliary substances - sea water - 250.0 mg, potassium dihydrogen phosphate - 0.45 mg, purified water - 754.35 mg or 753, 85 mg.
The theoretical total weight is 1005.3 mg.
Indications
Acute respiratory diseases with symptoms of rhinitis (runny nose), acute allergic rhinitis, hay fever, sinusitis, eustachitis, otitis media (to reduce swelling of the nasopharyngeal mucosa), to facilitate rhinoscopy and other diagnostic procedures in the nasal passages.
INN / Active ingredient
xylometazoline
Contraindications
Hypersensitivity to xylometazoline or any other component of the drug
arterial hypertension, tachycardia, severe atherosclerosis
increased intraocular pressure, especially angle-closure glaucoma
atrophic rhinitis, hyperthyroidism, surgical interventions on the meninges (in history), inflammatory diseases of the skin or mucous membrane of the vestibule of the nose, conditions after transsphenoidal hypophysectomy, pregnancy, children under 6 years of age (for 0.1% solution), children up to 2 x years (for 0.05% solution).
Do not use during therapy with monoamine oxidase (MAO) inhibitors (including 14 days after their withdrawal), tricyclic and tetracyclic antidepressants, other local vasoconstrictor agents (decongestants), as well as other drugs that increase blood pressure.
Storage conditions and periods
In a dry, dark place at a temperature not exceeding 25 ° C.
Keep out of the reach of children.
Specifications
Category
Runny nose
Scope of the medicinal product
Ear, Throat, Nose
Release form
Spray
Manufacturer country
Germany
Scope of application
Otorhinolaryngology
Minimum age from
6 years
Way of introduction
Nasally
Vacation conditions
Without recipe
Shelf life after opening
1 year
Volume, ml.
15 ml
Brand name
Stada
The amount of the dosage form in the primary package
15 ml
Primary packaging type
Spray bottle
Type of consumer packaging
Pack of cardboard
Pharmaco-therapeutic group
Decongestant - alpha adrenergic agonist
Anatomical and therapeutic characteristics
R01AA07 Xylometazoline
Dosage form
Nasal spray
Packaging
Cardboard box
Dosage (volume) of the substance in the preparation
xylometazoline hydrochloride 0.5 mg or 1.0 mg
Expiration date in days
1825
The target audience
Adult
Package weight, g
thirty
Mode of application
:
Intranasally.
Snoop® nasal spray 0.05%
For children aged 2 to 6 years, 1 injection into each nostril (if necessary, you can repeat it), up to three times a day.
Adults and children from 6 years of age, 2 sprays in each nostril, up to three times a day.
Snoop® nasal spray 0.1%
Adults and children from 6 years of age, 1 spray in each nostril (if necessary, you can repeat it), up to three times a day.
Snoop® nasal spray 0.1% should not be used in children under 6 years of age.
The drug should not be used more than 3 times a day, the duration of the course is no more than 7 days.
Before use, you must clean the nasal passages.
Remove the protective cap.
Before the first use, press the rim of the spray nozzle several times until a uniform cloud of fog" appears.
The vial with the drug is ready for further use
When using the nozzle, insert it into the nasal cavity and press the rim once.
Keep the bottle upright.
Do not spray horizontally or downward.
It is recommended to inhale slightly through the nose immediately after injection.
After use, close the bottle with a protective cap.
Each bottle must be used individually.
After completion of therapy, the drug can be re-prescribed only after a few days.
The duration of use in children should be consulted with a doctor.
In the case of chronic rhinitis, Snoop® 0.05% and 0.1% can only be used under medical supervision, given the risk of atrophy of the nasal mucosa.
If after treatment there is no improvement or the symptoms worsen, or new symptoms appear, you should consult your doctor.
Use the drug only according to the indications, the method of administration and the doses indicated in the instructions.
Information on technical characteristics, delivery set, country of manufacture "