FDA.reportPublic FDA data

Lexette 0.5 MG/ML Topical Foam

RxCUI
2106585
RxNorm name
Lexette 0.5 MG/ML Topical Foam
Display name
Lexette 0.5 MG/ML Topical Foam
Full name
Lexette 0.5 MG/ML Topical Foam
Term type
SY
Status
DailyMed mapping
Updated
2026-06-04 23:39:07

RxNav Current And Historical NDCs#

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No records found.

UNII Substances#

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No records found.

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
LEXETTEHALOBETASOL PROPIONATEMayne Pharma8aa1f819-c81f-4af1-aaa7-353df3203ff62025-05-31Warnings, Adverse reactionsExact identifier
rxcui: 2106585

DailyMed RxNorm Mappings#

unique DailyMed labels mapped to this RxNorm concept page 1 of 1 · 1 matching rows.

Set ID, RxNorm mappings, Terms table
Set IDRxNorm mappingsTermsSPL versionLabelEffective
8aa1f819-c81f-4af1-aaa7-353df3203ff6LEXETTE 0.05 % Topical Foam [PSN] · halobetasol propionate 0.5 MG/ML Topical Foam [Lexette] [SBD] · Lexette 0.05 % Topical Foam [SY] · Lexette 0.5 MG/ML Topical Foam [SY]41These highlights do not include all the information needed to use LEXETTE safely and effectively. See full prescribing information for LEXETTE. LEXETTE ® (halobetasol propionate) topical foam Initial U.S. Approval: 199020250531