US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Jan 14, 2022 (5 years ago)

Lexette (halobetasol propionate) Topical Foam, 0.05% 50 g canisters, Rx ONLY…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

CGMP Deviation: Difficulty dispensing/does not dispense or dispensing liquid instead of foam.

What was recalled

Lexette (halobetasol propionate) Topical Foam, 0.05% 50 g canisters, Rx ONLY, Distributed by: Mayne Pharma Greenville, NC 27834, NDC 51862-604-50

Recalling firm
Mayne Pharma Inc
NDC code
51862-604-50
Origin
NC, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0387-2022

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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