Full Prescribing Information Instructions for Use Patient Information Patient Site Request Samples
Goes to the Full Prescribing Information page Full Prescribing Information Goes to Instructions for Use page Instructions for Use Goes to the Patient Information page Patient Information Goes to the Patient Site Patient Site Goes to the Request Samples Page Request Samples
Goes to the Home page XHANCE® (fluticasone propionate) nasal spray 93 mcg logo
  • Home
  • Clinical Trial Results
    • Efficacy
    • Safety
  • Exhalation Delivery System
  • Dosing & Administration
  • Affordability & Access
  • Resources
representation of the sinonasal cavity of a healthy adult

The chronic rhinosinusitis (CRS)
therapy approved for adults
with or without nasal polyps1

A CRS therapy
designed to
GO DEEP2,3

When standard sprays fall short,
consider XHANCE.4-9

Graphic representation of the sinonasal cavity of a healthy adult.

See how the Exhalation Delivery System™ works
See the clinical evidence
Learn about dosing & administration
Get affordability & access information
IMPORTANT SAFETY INFORMATION

INDICATIONS

XHANCE is a corticosteroid indicated for the treatment of:

  • Chronic rhinosinusitis with nasal polyps (CRSwNP) in adults.
  • Chronic rhinosinusitis without nasal polyps (CRSsNP) in adults.

IMPORTANT SAFETY INFORMATION

CONTRAINDICATIONS:

Hypersensitivity to any ingredient in XHANCE.

WARNINGS AND PRECAUTIONS:

  • Local nasal adverse reactions, including epistaxis, erosion, ulceration, and septal perforation can occur. Monitor patients periodically for signs of possible changes on the nasal mucosa. If a septal perforation is noted, discontinue XHANCE. Candida infections may also occur with treatment with XHANCE which may require treatment with appropriate local therapy and discontinuation of XHANCE. Patients who have experienced recent nasal ulcerations, nasal surgery, or nasal trauma should not use XHANCE until healing has occurred.
  • Glaucoma and cataracts may occur with long-term use. Consider referral to an ophthalmologist in patients who develop ocular symptoms or use XHANCE long-term. Instruct patients to notify their healthcare provider if a change in vision occurs.
  • Hypersensitivity reactions (e.g., anaphylaxis, angioedema, urticaria, contact dermatitis, rash, hypotension, and bronchospasm) have been reported after administration of fluticasone propionate. Discontinue XHANCE if such reactions occur.
  • Immunosuppression and infections can occur, including potential increased susceptibility to or worsening of infections (e.g., existing tuberculosis; fungal, bacterial, viral, or parasitic infection; ocular herpes simplex). Use with caution in patients with these infections. More serious or even fatal course of chickenpox or measles can occur in susceptible patients. Corticosteroids should be used with caution, if at all, in patients with active or quiescent tuberculosis infections of the respiratory tract; systemic fungal, bacterial, viral, or parasitic infections; or ocular herpes simplex.
  • Hypercorticism and adrenal suppression may occur with very high dosages or at the regular dosage in susceptible individuals. If such changes occur, discontinue XHANCE slowly. Observe patients postoperatively or during periods of stress for evidence of inadequate adrenal response. The replacement of a systemic corticosteroid with a topical corticosteroid can be accompanied by signs of adrenal insufficiency. Inform patients that deaths due to adrenal insufficiency have occurred during and after transfer from systemic corticosteroids. Taper patients slowly from systemic corticosteroids if transferring to XHANCE.
  • Use with strong cytochrome P450 3A4 inhibitors (e.g., ritonavir, atazanavir, clarithromycin, indinavir, itraconazole, nefazodone, nelfinavir, saquinavir, ketoconazole, telithromycin, conivaptan, lopinavir, voriconazole) is not recommended because increased systemic corticosteroid adverse effects may occur.
  • Decreases in bone mineral density have been observed with long-term oral inhalation of products containing corticosteroids into the lungs. Assess initially and periodically thereafter in patients at high risk for decreased bone mineral content, such as prolonged immobilization, family history of osteoporosis, postmenopausal status, tobacco use, advanced age, poor nutrition, or chronic use of drugs that can reduce bone mass (e.g., anticonvulsants, oral corticosteroids).
  • Nasal corticosteroids, including XHANCE, may cause a reduction in growth velocity when administered to pediatric patients. The safety and effectiveness of XHANCE has not been established in pediatric patients.

ADVERSE REACTIONS:

Chronic rhinosinusitis with nasal polyps: The most common adverse reactions (incidence ≥ 3%) are epistaxis, nasal septal ulceration, nasopharyngitis, nasal mucosal erythema, nasal mucosal ulcerations, nasal congestion, acute sinusitis, nasal septal erythema, headache, and pharyngitis.

Chronic rhinosinusitis without nasal polyps: The most common adverse reactions (incidence ≥ 3%) are epistaxis, headache, and nasopharyngitis.

USE IN SPECIFIC POPULATIONS:

Hepatic impairment. Monitor patients for signs of increased drug exposure.


Please see Full Prescribing Information pdf opensfull Prescribing Information, including Patient Information pdf opensPatient Information, for XHANCE.

References
  1. Full Prescribing Information for XHANCE (fluticasone propionate). OptiNose US, Inc.; 2024.
  2. Djupesland PG, Skretting A, Winderen M, Holand T. Breath actuated device improves delivery to target sites beyond the nasal valve. Laryngoscope. 2006;116(3):466-472.
  3. Djupesland PG, Skretting A. Nasal deposition and clearance in man: comparison of a bidirectional powder device and a traditional liquid spray pump. J Aerosol Med Pulm Drug Deliv. 2012;25(5):280-289.
  4. Data on file. Study 3205. Paratek Pharmaceuticals, Inc.
  5. Data on file. Study 3206. Paratek Pharmaceuticals, Inc.
  6. Sindwani R, Han JK, Soteres DF, et al. NAVIGATE I: randomized, placebo-controlled, double-blind trial of the exhalation delivery system with fluticasone for chronic rhinosinusitis with nasal polyps. Am J Rhinol Allergy. 2019;33(1):69-82.
  7. Leopold DA, Elkayam D, Messina JC, Kosik-Gonzalez C, Djupesland PG, Mahmoud RA. NAVIGATE II: randomized, double-blind trial of the exhalation delivery system with fluticasone for nasal polyposis. J Allergy Clin Immunol. 2019;143(1):126-134.e5.
  8. Data on file. Study 3101. Paratek Pharmaceuticals, Inc.
  9. Data on file. Study 3102. Paratek Pharmaceuticals, Inc.
  • Contact Us
  • Privacy Policy
  • Terms of Use
  • Site Map

This site is intended for healthcare professionals in the United States.
PARATEK®, the hexagon logo, XHANCE®, EDS®, and Exhalation Delivery System™
are trademarks of Paratek Pharmaceuticals, Inc. and/or its affiliated companies.

Click to go to the Paratek Pharmaceuticals web site Paratek® logo
©2025 Paratek Pharmaceuticals, Inc. All rights reserved.  US-XHA-0056 12/25

Are you a US healthcare professional?

Click to reject No

You are about to leave the XHANCE HCP website.

Are you sure?

Click to accept Yes