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Local Anaesthetic (Amide) Pregnancy: There is no, or inadequate evidence of safety of the drug in human pregnancy but it has been in wide use for many years without apparent ill consequence, and animal studies have shown no hazard. If drug therapy is needed in pregnancy, this drug can be used if there is no safer alternative. Breast-feeding: Lidocaine enters the mother's milk, but in such small quantities that there is generally no risk of the child being affected at therapeutic dose levels.

Lidocaine (Intranasal/Topical ENT)

Brand names: Xylocaine 10% Spray

Topical lidocaine applied to the nasal or upper airway mucosa as a spray or applied solution provides local anaesthesia of the ENT mucosa before procedures such as nasendoscopy, nasal packing or biopsy.

Adult dose

Dose: Xylocaine 10 mg Spray (lidocaine 10 mg per metered dose; each activation of the metered dose valve delivers 10 mg lidocaine base), surface anaesthesia before minor non-invasive procedures in the nasal cavity, pharynx and epipharynx (including rhinoscopy and laryngoscopy) and before insertion of instruments and catheters into the respiratory and digestive tract: the number of sprays depends on the extent of the area to be anaesthetised; up to 20 applications (200 mg lidocaine base) for procedures in the pharynx, larynx and trachea; no more than 20 spray applications in any adult
Route: Topical spray to the mucosa (nasal cavity, pharynx, epipharynx, larynx), using the supplied single-patient nozzle
Frequency: Single application as required for the procedure; the SPC prints no repeat interval ('Excessive dosage, or short intervals between doses, may result in high plasma levels and serious adverse effects')
Max: No more than 20 spray applications (10 mg lidocaine base each) in any adult
§2 (verbatim): 'Lidocaine 10 mg/metered dose. Excipient(s) with known effect: Each depression also delivers 1 mg of propylene glycol (an excipient of the banana essence). Also contains ethanol.' The SPC prints '10 mg/metered dose'; it does not print a percentage or mg/mL concentration. §4.1 (verbatim, ENT and related uses): 'Otorhinolaryngology Anaesthesia prior to minor non-invasive procedures in the nasal cavity, pharynx and epipharynx including rhinoscopy and laryngoscopy.' 'Insertion of instruments and catheters into the respiratory and digestive tract Provides surface anaesthesia for the oropharyngeal and tracheal areas to reduce reflex activity, attenuate haemodynamic response and to facilitate insertion of the catheter or the passage of instruments during endotracheal intubation, laryngoscopy, bronchoscopy, oesophagoscopy and gastroscopy.' General: 'This product is non-sterile and therefore not recommended for use prior to procedures that require aseptic techniques.' The SPC also lists obstetric supplementary pain control and dental practice, which are not this page's use and are not dosed here. VERBATIM §4.2: 'As with any local anaesthetic, reactions and complications are best averted by employing the minimal effective dosage. Debilitated or elderly patients and children should be given doses commensurate with their age and physical condition.' 'Each activation of the metered dose valve delivers 10 mg lidocaine base. It is unnecessary to dry the site prior to application. No more than 20 spray applications should be used in any adult to produce the desired anaesthetic effect. The number of sprays depend on the extent of the area to be anaesthetised.' For dental practice it prints '1–5 applications to the mucous membranes' and for obstetrics 'Up to 20 applications (200 mg lidocaine base)' (neither is this page's use); for 'Insertion of instruments and catheters into the respiratory and digestive tract Up to 20 applications (200 mg lidocaine base) for procedures in pharynx, larynx, and trachea.' The SPC prints NO separate spray count for the nasal cavity, pharynx or epipharynx uses beyond the general adult limit of 20 sprays, and no per-spray count specific to nasoendoscopy; the figures above are the only ones printed. Method (§4.2): 'Xylocaine spray is administered using the supplied nozzle. ... Nozzles are non- sterile single patient single use only. Appropriate measures should be undertaken to avoid cross contamination (see Section 6.6).' 'Xylocaine Spray should not be used on cuffs of endotracheal tubes (ETT) made of plastic (see also section 4.4).' NO PAEDIATRIC DOSE is printed in the SPC (only 'children should be given doses commensurate with their age and physical condition'), so none is written. ASPIRATION (§4.4): 'The oropharyngeal use of topical anaesthetic agents may interfere with swallowing and thus enhance the danger of aspiration. This is particularly important in children because of their frequency of eating. Numbness of the tongue or buccal mucosa may increase the danger of biting trauma.' ABSORPTION (§4.4): 'Absorption from mucous membranes is variable but is especially high from the bronchial tree. Such applications may therefore result in rapidly rising or excessive plasma concentrations, with an increased risk of toxic symptoms, such as convulsions.' The SPC prints no fasting interval after use, so none is stated.

Dose adjustments

Renal

No numerical renal dose adjustment is printed. §4.4: lidocaine 'should be used with caution' in patients with severe renal dysfunction if the dose or site of administration is likely to result in high blood levels.

Hepatic

No numerical hepatic dose adjustment is printed. §4.4: lidocaine 'should be used with caution' in patients with impaired hepatic function if the dose or site of administration is likely to result in high blood levels; unparalysed patients are more likely to swallow a large proportion of the dose, which then undergoes considerable first-pass hepatic metabolism following absorption from the gut.

Dose independently re-sourced from UK Summary of Product Characteristics (SPC) via MHRA Products — clinician-reviewed. Always confirm against the product SmPC and your local formulary before prescribing.

Contraindications

  • Hypersensitivity to the active substance, to any of the excipients listed in section 6.1 or to local anaesthetics of the amide-type (§4.3)

Side effects

  • In extremely rare cases amide-type local anaesthetic preparations have been associated with allergic reactions (in the most severe instances anaphylactic shock) (§4.8)
  • Local irritation at the application site has been described (§4.8)
  • Following application to laryngeal mucosa before endotracheal intubation: reversible 'sore throat', 'hoarseness' and 'loss of voice' have been reported; the spray provides surface anaesthesia during an endotracheal procedure but does not prevent post-intubation soreness (§4.8)
  • Systemic adverse reactions are rare and may result from high plasma levels due to excessive dosage or rapid absorption (e.g. following application to areas below the vocal chords) or from hypersensitivity, idiosyncrasy or reduced tolerance; they involve the central nervous system and/or the cardiovascular system (§4.8)
  • CNS reactions are excitatory and/or depressant: nervousness, dizziness, convulsions, unconsciousness and possibly respiratory arrest; the excitatory reactions may be very brief or may not occur at all, in which case the first manifestations of toxicity may be drowsiness, merging into unconsciousness and respiratory arrest (§4.8)
  • Cardiovascular reactions are depressant: hypotension, myocardial depression, bradycardia and possibly cardiac arrest (§4.8)
  • Oropharyngeal use may interfere with swallowing and enhance the danger of aspiration; numbness of the tongue or buccal mucosa may increase the danger of biting trauma (§4.4)

Interactions

  • Other local anaesthetics or agents structurally related to amide-type local anaesthetics, e.g. antiarrhythmic drugs such as mexiletine: use with caution since the toxic effects are additive (§4.5)
  • Class III antiarrhythmic drugs (e.g. amiodarone): specific interaction studies have not been performed, but caution is advised; patients should be under close surveillance and ECG monitoring considered, since cardiac effects may be additive (§4.4, §4.5)
  • Drugs that reduce the clearance of lidocaine (e.g. cimetidine or beta-blockers): may cause potentially toxic plasma concentrations when lidocaine is given in repeated high doses over a long time period; such interactions should be of no clinical importance following short-term treatment at recommended doses (§4.5)

Monitoring

  • Use the minimal effective dosage; excessive dosage, or short intervals between doses, may result in high plasma levels and serious adverse effects (§4.2, §4.4)
  • Caution in patients with wounds or traumatised mucosa in the region of the proposed application: damaged mucosa will permit increased systemic absorption (§4.4)
  • Special attention in patients with epilepsy, cardiovascular disease and heart failure, impaired cardiac conduction or bradycardia, severe renal dysfunction, impaired hepatic function, severe shock, the elderly and patients in poor general health, if the dose or site of administration is likely to result in high blood levels (§4.4)
  • Resuscitative equipment, oxygen and other resuscitative drugs should be available for the management of serious adverse reactions (§4.4)
  • In paralysed patients under general anaesthesia, higher blood concentrations may occur than in spontaneously breathing patients (§4.4)
  • Aspiration risk after oropharyngeal use, particularly in children; risk of biting trauma while the tongue or buccal mucosa is numb (§4.4)
  • Avoid contact with the eyes (§4.4)
  • Do not use on cuffs of plastic endotracheal tubes: lidocaine base may damage both PVC and non-PVC cuffs (pinholes causing leakage and pressure loss) (§4.4)
  • Probably porphyrinogenic: prescribe to patients with acute porphyria only on strong or urgent indications, with appropriate precautions (§4.4)

Clinical monograph

How it works

Lidocaine is an amide local anaesthetic that reversibly blocks voltage-gated sodium channels in sensory nerve endings, preventing impulse conduction and thereby abolishing local pain sensation.

Prescribing in practice

  • Systemic absorption across inflamed or highly vascular mucosa can be rapid, so respect the maximum recommended cumulative dose to avoid local-anaesthetic systemic toxicity (CNS excitation then depression, arrhythmias).
  • Anaesthesia of the pharynx and larynx abolishes the gag reflex and impairs swallowing, increasing aspiration risk until sensation returns.
  • Use with caution in patients with epilepsy, conduction abnormalities, hepatic impairment or porphyria, and have resuscitation facilities available for airway application.

Monitoring

Observe for early signs of systemic toxicity (peri-oral tingling, light-headedness, visual or auditory disturbance) and protect the airway until pharyngeal sensation and the gag reflex recover.

Counselling the patient

  • Do not eat or drink until the numbness in your throat has fully worn off, to avoid choking.
  • A bitter taste and temporary throat numbness are expected after spraying.
  • Tell the clinician if you feel dizzy, develop tingling around the mouth or notice a ringing in your ears.

Evidence & guidelines

Topical lidocaine is a long-established standard for mucosal anaesthesia in ENT and airway procedures, with dosing and safety limits defined in the SPC and current prescribing references.

Reference: AAGBI LAST Guidelines; ENT-UK Procedural Guidance; Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. The structured dose values shown have been reviewed by a clinician. Monograph status: clinician-reviewed (2026-07-04).

Related

Curated clinical cross-links plus same-class fallbacks.