fluticasone nasal
Brand names: Flonase
Fluticasone nasal spray helps relieve allergy symptoms. It belongs to a class of drugs called nasal corticosteroids.
What it does
This medicine treats allergy symptoms.
Common side effects
No common side effects listed.
Key warnings
Children under 12 years of age should not use this medicine.
How It Works
This drug is a nasal corticosteroid. It works by reducing inflammation in the nose. This helps to relieve allergy symptoms.
How to Take It
Do not use more medicine than directed. Adults and children 12 years and older can take 1 tablet (2.5 mg) every 4 to 6 hours. Do not take more than 4 tablets (10 mg) in 24 hours. Follow your doctor's directions.
Pregnancy & Breastfeeding
There is not enough information available about the safety of this drug during pregnancy or breastfeeding. Talk to your doctor before using this medicine if you are pregnant or breastfeeding.
Missed Dose
Since this medicine is taken as needed, you likely won't miss a dose. If you are taking it regularly and miss a dose, take it as soon as you remember. Skip the missed dose if it is almost time for your next dose.
Storage
Store this medicine at room temperature between 68-77°F (20-25°C).
Serious Warnings
Children under 12 years of age should not use this medicine.
Common Questions
What is fluticasone nasal spray used for?
How often can I use this medicine?
Can children under 12 use this medicine?
What should I do if I miss a dose?
How should I store this medicine?
Is this medicine safe to use during pregnancy?
Can I use this medicine if I am breastfeeding?
What if I accidentally use too much?
Does this medicine have any side effects?
Can I take this with other allergy medicines?
What drug class is fluticasone nasal?
Is fluticasone nasal safe during pregnancy?
Related Medications in Nasal Corticosteroid
Other drugs grouped near fluticasone nasal — same-class peers and common alternatives.
azelastine
Astelin, Astepro
Azelastine nasal spray is an antihistamine medicine.
Compare with fluticasone nasal →
budesonide nasal
Rhinocort
Rhinocort is a nasal spray that helps relieve allergy symptoms.
Compare with fluticasone nasal →
cetirizine
Zyrtec
Cetirizine (Zyrtec) is an antihistamine medicine.
Compare with fluticasone nasal →
chlorpheniramine
Chlor-Trimeton
Chlorpheniramine is an antihistamine medicine.
Compare with fluticasone nasal →
ciclesonide nasal
Omnaris, Zetonna
Omnaris Nasal Spray is a medicine that helps treat allergy symptoms in your nose.
Compare with fluticasone nasal →
Medication Guides
Understanding Drug Interactions
How CYP450 enzymes, inhibitors, and inducers affect your medications
Generic vs Brand Name Drugs
FDA requirements, cost savings, and when the difference matters
Pain Relievers Compared
NSAIDs vs acetaminophen — which OTC pain reliever to use
Narrow Therapeutic Index Drugs
Why some drugs demand precise dosing and monitoring
Common Drug Interactions
Dangerous medication combinations and how to protect yourself
Related Health & Safety Data
🩺 Find a Doctor
Search prescribers for Nasal Corticosteroid
🏨 Hospital Quality
CMS hospital ratings, safety scores & patient outcomes
💊 Supplement Data
NIH DSLD — check supplement ingredients & label claims
🍽️ Food Safety Alerts
FDA recalls, inspections & outbreak investigations
⚠️ Product Recalls
FDA, CPSC & NHTSA recall search
💉 Procedure Costs
Medicare procedure pricing for 9,297 procedures
What the FDA Data Shows for fluticasone nasal
The FDA label for fluticasone nasal (sold under brand names such as Flonase) classifies it as an over-the-counter product in the Nasal Corticosteroid class. This medicine treats allergy symptoms. Labeling covers dosing, contraindications, and monitoring requirements derived from clinical trials.
Post-market surveillance from the FDA Adverse Event Reporting System (FAERS) captures real-world experience. Voluntary reports accumulate over the lifetime of a drug and reflect wide-ranging clinical use. Interaction data is drawn directly from FDA-approved prescribing information. Acquisition-cost data is surveyed weekly by CMS and updated as manufacturers report changes.
Report counts do not establish causation — a FAERS entry documents a temporal association, not proof that the drug produced the outcome. Widely prescribed medications naturally accumulate more reports than niche therapies, so raw totals must be interpreted alongside total exposure. Shortage status, recall history, and patent information further shape supply and switching decisions. This page summarizes public FDA data for educational purposes only and is not a substitute for professional medical advice — always consult a licensed healthcare provider before starting, stopping, or changing any medication.
Data Sources
Drug labeling: FDA Drug Labels (SPL/DailyMed). Adverse events: FDA Adverse Event Reporting System (FAERS).
FAERS reports are voluntary and do not establish causation. Drug interactions are derived from FDA labeling and clinical references. Always consult a healthcare professional before making medication decisions.
Last updated: October 2, 2024
Read our methodology — how this data is sourced, computed, and verified.
All federal data sources used on this page
- FDA Orange Book — approved drug products with therapeutic equivalence. accessdata.fda.gov/cder/ob
- FDA DailyMed — NIH-hosted drug labeling for FDA-approved meds. dailymed.nlm.nih.gov
- FDA Adverse Event Reporting System (FAERS) — post-marketing safety surveillance. fda.gov/drugs/faers
- NLM RxNorm — standardized clinical drug nomenclature. nlm.nih.gov/research/umls/rxnorm
- CMS Medicare Part B Drug Average Sales Price Files — federal drug pricing data. cms.gov/medicare/part-b-drugs/asp
- FDA Drug Shortages Database — current and resolved drug shortage tracking. accessdata.fda.gov/drugshortages