TRPV1 Agonist (Nasal Desensitisation Agent)
Pregnancy: Avoid — insufficient data; localised nasal absorption is minimal but lack of pregnancy safety data precludes recommendation
Capsaicin Nasal Spray
Brand names: Rhinopasic (0.1 mmol/L)
Adult dose
Dose: One spray (0.1 mmol/L) to each nostril for 3 sessions on 1 day per week over 3 weeks (3 total treatment days)
Route: Intranasal spray
Frequency: Once per treatment day (3 treatment days, 1 week apart)
Max: 3 treatment sessions
Non-allergic rhinitis (idiopathic/vasomotor rhinitis) unresponsive to other treatments; MHRA licensed 2023 as Rhinopasic; initial burning sensation — premedicating with lidocaine spray reduces discomfort; pre-treat with nasal saline
Paediatric dose
Dose: Not established N/A/kg
Route: N/A
Frequency: N/A
Max: N/A
Not licensed in paediatrics
Dose adjustments
Renal
No systemic dose adjustment required
Hepatic
No systemic dose adjustment required
Paediatric weight-based calculator
Not licensed in paediatrics
Clinical pearls
- Mechanism: capsaicin activates TRPV1 channels on unmyelinated C-fibres in the nasal mucosa → initial neurogenic inflammation → prolonged desensitisation of C-fibres and depletion of substance P; results in reduced neurogenic inflammation and improved non-allergic rhinitis symptoms
- MHRA 2023 approved as Rhinopasic for idiopathic non-allergic rhinitis — first licensed nasal capsaicin product in UK; previously used off-label as homemade preparations; highly concentrated pharmaceutical formulation provides standardised dose
- Non-allergic rhinitis (vasomotor rhinitis) affects up to 30% of rhinitis patients — not IgE mediated; symptoms triggered by temperature changes, odours, humidity, exercise; antihistamines ineffective (no allergic component); capsaicin targets the neurogenic pathway
- Duration of effect: clinical trials show symptom improvement lasting 3-6 months after 3-treatment course; can be repeated; patients typically notice benefit within 2-4 weeks post-treatment
- Patient counselling key to adherence: the initial burning is alarming but expected and temporary — explaining this before administration dramatically improves completion rates; saline pre-spray and asking patient to breathe through mouth during application helps
Contraindications
- Allergic rhinitis (not effective — for non-allergic only)
- Nasal polyps (not studied)
- Active nasal infection
- Known capsaicin hypersensitivity (hot chilli allergy)
Side effects
- Nasal burning/stinging during and shortly after application (expected — subsides within 20-30 minutes)
- Watery eyes
- Sneezing
- Rhinorrhoea immediately post-application
- Transient cough
Interactions
- No pharmacological interactions — localised nasal action
Monitoring
- Symptom response at 4 weeks (TNSS/VAS)
- Tolerability of burning (first treatment session)
- No routine laboratory monitoring required
Reference: BNFc; BNF 90; Fokkens et al. EPOS 2020; Bernstein et al. Laryngoscope 2011; MHRA SPC Rhinopasic 2023; Baudoin et al. J Allergy Clin Immunol 2019. Verify against your local formulary and the latest BNF before prescribing.
Related
Curated clinical cross-links plus same-class fallbacks.
Calculators
Pathways
- Adult Upper Airway Obstruction (Stridor) · DAS 2015 unanticipated difficult airway; RCEM
- Epistaxis Management · ENT-UK / NICE
- Acute Otitis Media · NICE NG91 2018
- Tonsillitis and Sore Throat · NICE NG84 2018
- Benign Paroxysmal Positional Vertigo · NICE CG124 / AAO-HNS Guidelines
- Acute Rhinosinusitis · NICE NG79 2017 / EPOS 2020