Regulatory UpdatesSep 27, 2026•1 min read

FDA NDA018363: HEXASCRUB Topical Sponge Discontinued

By the PharmaCountry team

The FDA lists HEXASCRUB, a 3% hexachlorophene topical sponge, under application NDA018363 with a discontinued marketing status. Sponsor: PROF DSPLS.

The U.S. Food and Drug Administration (FDA) has recorded the status of HEXASCRUB under application number NDA018363. HEXASCRUB is a topical product delivered via a sponge, containing 3% hexachlorophene as its active ingredient. The sponsor for this application is PROF DSPLS. According to the FDA database, the product’s marketing status is listed as discontinued. No reference drug or reference standard is associated with this submission, and the product is not classified as a reference drug. The product’s route of administration is topical, and it is not currently marketed.

Compiled by the PharmaCountry team · Source: FDA.gov

Topics:#FDA #NDA018363 #HEXASCRUB #hexachlorophene #topical #discontinued