Active Ingredient (In Each Spray)
Fluticasone furoate 27.5 mcg (glucocorticoid)*
*read the Question & Answer Book
The following Structured Product Label (SPL) was submitted to the FDA by A-s Medication Solutions for the product Flonase Sensimist (NDC 50090-5967). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient (in each spray), purpose, uses, warnings, do not use, ask a doctor before use if you, ask a doctor or pharmacist before use if you are taking, when using this product, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Fluticasone furoate 27.5 mcg (glucocorticoid)*
*read the Question & Answer Book
Allergy symptom reliever
Temporarily relieves these symptoms of hay fever or other upper respiratory allergies:
Only for use in the nose. Do not spray into your eyes or mouth.
have or had glaucoma or cataracts
ask a health professional before use.
In case of overdose, get medical help or contact a Poison Control Center right away.
ADULTS AND CHILDREN 12 YEARS OF AGE AND OLDER
CHILDREN 2 TO 11 YEARS OF AGE
CHILDREN UNDER 2 YEARS OF AGE
benzalkonium chloride solution, carboxymethylcellulose sodium, dextrose anhydrous, edetate disodium, microcrystalline cellulose, polysorbate 80, purified water
call toll-free 1-844-FLONASE (1-844-356-6273)
Product: 50090-5967
NDC: 50090-5967-0 60 SPRAY, METERED in a BOTTLE / 1 in a PACKAGE
* Please review the disclaimer below.