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Mentholatum (China) Pharmaceuticals Co., Ltd.

FDA Regulatory Profile

Mentholatum (China) Pharmaceuticals Co., Ltd. has 0 FDA recalls, 3 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Aug 15, 2025 · VAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 4, 2026 (checked Nov 8, 2026, unchanged)File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections3Nov 10, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Aug 15, 2025Zhongshan, ChinaDrugsVoluntary Action Indicated (VAI)3000188423
Jun 21, 2019Zhongshan, ChinaDrugsVoluntary Action Indicated (VAI)3000188423
Apr 10, 2015Zhongshan, ChinaDrugsVoluntary Action Indicated (VAI)3000188423

NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.

FDA-Inspected Facilities

FacilityLocationInspectionsLatest
FEI 3000188423Zhongshan, China3Aug 15, 2025

FDA data resources

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.