Active Ingredient(S)
Fluticasone propionate (glucocorticoid) 50 mcg per spray
The following Structured Product Label (SPL) was submitted to the FDA by Allegiant Health for the product Fluticasone Propionate (NDC 69168-014). 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(s), purpose, use(s), warnings, do not use, ask a doctor before use if you, ask a doctor or pharmacist before use if, when using this product, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Fluticasone propionate (glucocorticoid) 50 mcg per spray
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 (1-800-222-1222) right away.
read the Quick Start Guide for how to:
ADULTS AND CHILDREN 12 YEARS OF AGE AND OLDER
CHILDREN 4 to 11 YEARS OF AGE
CHILDREN UNDER 4 YEARS OF AGE: do not use
0.02% w/w benzalkonium chloride, dextrose, microcrystalline cellulose and carboxymethylcellulose sodium, 0.25% w/w phenylethyl alcohol, polysorbate 80, purified water
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