Label: FLUTICASONE PROPIONATE NASAL- fluticasone propionate spray, metered
- NDC Code(s): 59368-342-01
- Packager: Praxis, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated January 1, 2023
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Active ingredient (in each spray)Fluticasone propionate (glucocorticoid) 50 mcg
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PurposeAllergy symptom reliever
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UsesTemporarily relieves these symptoms of hay fever or other upper respiratory allergies: nasal congestion - runny nose - sneezing - itchy nose - itchy, watery eyes
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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 fully ...
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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 ...
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Other informationyou may start to feel relief the first day and full effect after several days of regular, once-a-day use - store between 4 - oand 30 - oC (39 - oand 86 - oF) keep this package ...
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Inactive ingredientsbenzalkonium chloride, dextrose, microcrystalline cellulose, phenylethyl alcohol, polysorbate 80, purified water, sodium carboxymethylcellulose
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Questions or comments?1-800-719-9260
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