RYALTRIS NASAL SPRAY 600/25MCG [SIN16523P]
Active ingredients: RYALTRIS NASAL SPRAY 600/25MCG
Product Info
RYALTRIS NASAL SPRAY 600/25MCG
[SIN16523P]
Product information
Active Ingredient and Strength | MOMETASONE FUROATE MONOHYDRATE (MICRONIZED) EQV TO MOMETASONE FUROATE - 25 MCG/SPRAY |
Dosage Form | SPRAY, SUSPENSION |
Manufacturer and Country | GLENMARK PHARMACEUTICALS LIMITED (BADDI SITE) - INDIA |
Registration Number | SIN16523P |
Licence Holder | LOTUS INTERNATIONAL PTE. LTD. |
Forensic Classification | PRESCRIPTION ONLY MEDICINES |
Anatomical Therapeutic Chemical (ATC) code | R01AD59 |
Prescription-only Medicines with Exemptions for Supply without Prescription | NA |
Indication
INDICATIONS
RYALTRIS® is indicated for the treatment of moderate to severe symptoms associated with allergic rhinitis and rhinoconjunctivitis in patients 6 years of age and older.
Dosing
DOSAGE AND ADMINISTRATION
Dosage
Adults and Adolescents (12 Years of Age and Older)
The recommended dosage of RYALTRIS® is 2 sprays in each nostril twice daily.
Children (6 to 11 Years of Age)
The recommended dosage of RYALTRIS® is 1 spray in each nostril twice daily.
Paediatric
In children 6 to 11 years of age, safety of RYALTRIS® beyond 2 weeks of use has not been assessed.
The safety and effectiveness of RYALTRIS® in paediatric patients below the age of 6 years has not been established.
Administration
Administer RYALTRIS® by the intranasal route only. Avoid spraying RYALTRIS® into the eyes or mouth.
Shake the bottle well before each use.
Priming: Prime RYALTRIS® before initial use by releasing 6 sprays. When RYALTRIS® has not been used for 14 days or more, re-prime by releasing 2 sprays or until a fine mist appears.
Missed Dose
If a single dose is missed, the next dose should be taken when it is due. A double dose should not be taken at the same time.
Contraindications
CONTRAINDICATIONS
RYALTRIS® is contraindicated for patients who:
Are hypersensitive to this medicine or to any ingredient in the formulation, including any non-medicinal ingredient, or component of the container. For a complete listing, see Qualitative and Quantitative Composition – please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information.
Have untreated fungal, bacterial, or tuberculosis infections of the respiratory tract.
