Ballicules › Drugs › Benzonatate
Pronunciation: ben-ZOE-na-tayt
Mechanism of action: Benzonatate ballicule
What it is Peripheral antitussive that anesthetizes airway stretch receptors; symptomatic treatment of cough.
Why this one It suppresses cough without opioid dependence or routine sedation, but benefit is often modest.
What limits it ⚑ Swallow capsules whole: chewing can anesthetize the mouth and compromise the airway. Small pediatric overdoses can be rapidly fatal.
Molecular structure: Benzonatate
FDA-approved for
FDA label
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FDA dosing Population Start Target Max
Cough (symptomatic relief) Adults & children >10 yr 100-200 mg TID PRN 100-200 mg TID PRN 600 mg/day in 3 divided doses
Renal Undefined
Hepatic Undefined
Instructions Swallow capsule whole; do not break, chew, dissolve, cut, or crush (risk of oropharyngeal anesthesia, laryngospasm, cardiovascular collapse)
Available strengths
Cautions Severe hypersensitivity reactions (bronchospasm, laryngospasm, cardiovascular collapse) possible if chewed/sucked Accidental or intentional overdose can be fatal, particularly in children
Adverse reactions CNS: sedation, headache, dizziness, mental confusion, visual hallucinations GI: constipation, nausea, GI upset Hypersensitivity, pruritus, skin eruptions Nasal congestion, burning eyes, numbness of chest
Pregnancy Category C — animal studies not conducted; use only if clearly needed
Lactation Undefined
Cost Benzonatate (TESSALON)
What pharmacies pay · NADAC 9/30/26
Strength #/mo generic $/mo CostPlus 100 mg cap 90 TID $5.90 offered 150 mg cap 90 TID not offered 200 mg cap 90 TID $9.12 offered
Generic entry 1993
Principal risk Fatal in overdose in children; never chew the capsule
Classes and tags
Clinical profile
Therapeutic safety burden 1 / 4
Overdose danger 3 / 4
Weight-gain liability 0 / 4
Sedation liability 0 / 4
QT / Torsades 0 / 4
Direct muscarinic antagonism 0 / 4
Embryofetal risk 1 / 4
Legacy pregnancy category Unknown / historical label unavailable
Defining liability Generally tolerated at therapeutic doses; clinically important risks are agent-specific and increase with interactions or organ impairment.
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