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Treats molluscum contagiosum. Sold as Ycanth. Every FDA application for this active ingredient.
As of Nov 14, 2026, FDA lists 1 application for Cantharidin (sold as Ycanth), first approved Jul 21, 2023, with 0 new uses approved and 3 published complete response letters.
First approved: Jul 21, 2023
Applications: 1
New uses approved: 0
Complete response letters: 3
Medicare spending, 2025: $54K
First approved in Japan: Sep 19, 2025
Medicare Spending
CMS Part D and Part B, 2025, before manufacturer rebates; matched by generic name
First approved in Japan 26 months after the US. PMDA's English list since 2008, matched by ingredient; see all Japanese approvals
Ycanth Topical, new ingredientA drug with a new active ingredient indicated for the treatment of molluscum contagiosum. · Torii Pharmaceutical Co., Ltd. · Sep 19, 2025
Clinical Trials
5 open or ongoing studies name this ingredient as an intervention, including as a comparator; newest first. See all
Applications, approvals and products come from FDA's Drugs@FDA data files, refreshed weekly, grouped by active ingredient as FDA spells it. Complete response letters are FDA's published letters. Medicare spending is CMS's Part D and Part B dashboard, matched to this ingredient by generic name; shortages are FDA's shortage list, matched by application number; clinical trials are ClinicalTrials.gov studies naming the ingredient as an intervention, refreshed daily; safety programs are FDA's REMS list, matched by application number or, for shared programs, by ingredient.Drugs@FDA
