Active Ingredient
Fluticasone propionate
(glucocorticoid) 50 mcg
The following Structured Product Label (SPL) was submitted to the FDA by Selder, S.a. De C.v. for the product Fluticasone Propionate (NDC 63654-380). 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, purpose, uses, warnings, do not use, ask a doctor before use if, 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 propionate
(glucocorticoid) 50 mcg
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
If pregnant or breast-feeding, ask a health professional before use.
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.
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
They contain important additional information.
0.02% w/w benzalkonium chloride, dextrose, microcrystalline cellulose and carboxymethylcellulose sodium, 0.25% w/w phenylethyl alcohol, polysorbate 80, purified water
Call toll free 1-888-952-0050 weekdays
8:30am - 5:00pm Eastern Standard Time
XL-3*
Allergy Cortix
FLUTICASONE PROPIONATE
NASAL SPRAY, USP
50 mcg Per Spray
Allergy Symptom Reliever
(Glucocorticoid
24 hour (icon) Non-Drowsy*
relief of:
Nasal congestion
Runny nose
Itchy nose
Sneezing
Full Prescription Strength
120 Metered Sprays
0.54 FL OZ (15.8mL)
* Please review the disclaimer below.