FDA.reportPublic FDA data

Ultravate 0.05 % Topical Lotion

RxCUI
1790329
RxNorm name
Ultravate 0.05 % Topical Lotion
Display name
Ultravate 0.05 % Topical Lotion
Full name
Ultravate 0.05 % Topical Lotion
Term type
SY
Status
DailyMed mapping
Updated
2026-06-04 23:39:03

RxNav Current And Historical NDCs#

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UNII Substances#

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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.

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Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ULTRAVATEHALOBETASOL PROPIONATELacer Pharma, LLC74e899db-1c1f-48b2-9913-5d32a14906ae2025-04-06Warnings, Adverse reactionsExact identifier
rxcui: 1790329

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
74e899db-1c1f-48b2-9913-5d32a14906aeUltravate 0.05 % Topical Lotion [PSN] · halobetasol propionate 0.5 MG/ML Topical Lotion [Ultravate] [SBD] · Ultravate 0.05 % Topical Lotion [SY]31These highlights do not include all the information needed to use ULTRAVATE® Lotion safely and effectively. See full prescribing information for ULTRAVATE Lotion. ULTRAVATE (halobetasol propionate) lotion, for topical use Initial U.S. Approval: 199020250406