Label: FLUTICASONE PROPIONATE spray, metered
- NDC Code(s): 55681-389-14
- Packager: TWIN MED LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated May 1, 2025
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
-
Active ingredient (in each spray)Fluticasone propionate - (glucocorticoid) 50 mcg
-
PurposeAllergy symptom reliever
-
UsesTemporarily relieves these symptoms of hay fever or other upper respiratory allergies: nasal congestion - runny nose sneezing - itchy nose - itchy watery eyes
-
WarningsOnly for use in the nose. Do not spray into your eyes or mouth. Do not use - in children under 4 years of age - to treat asthma - if you have an injury or surgery to your nose that is not ...
-
Directionsread the Quick Start Guide for how to: prime the bottle - use the spray - clean the spray nozzle - shake gently before each use - use this product only once a day - do not use more than directed - ADULTS ...
-
Other informationyou may start to feel relief the first day and full effect after several days of regular once-a-day use - store between 4º and 30ºC (39º and 86ºF) keep this label and enclosed materials. They ...
-
Inactive ingredients0.02% w/w benzalkonium chloride, dextrose, microcrystalline cellulose and carboxymethylcellulose sodium, 0.25% w/w phenylethyl alcohol, polysorbate 80, purified water
-
Questions or commentsCall toll-free 1-800-935-6737
-
Principal Display Panel-Label
-
Principal Display Panel-Carton
-
INGREDIENTS AND APPEARANCEProduct Information