FDA.reportPublic FDA data

Wynzora (calcipotriene 0.005 % / betamethasone dipropionate 0.064 % ) Topical Cream

RxCUI
2471878
RxNorm name
Wynzora (calcipotriene 0.005 % / betamethasone dipropionate 0.064 % ) Topical Cream
Display name
Wynzora (calcipotriene 0.005 % / betamethasone dipropionate 0.064 % ) Topical Cream
Full name
Wynzora (calcipotriene 0.005 % / betamethasone dipropionate 0.064 % ) Topical Cream
Term type
SY
Status
DailyMed mapping
Updated
2026-06-04 23:38:54

RxNav Current And Historical NDCs#

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UNII Substances#

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openFDA label cross-check#

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Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
WynzoraCALCIPOTRIENE AND BETAMETHASONE DIPROPIONATEMC2 Therapeutics Ltd36c5c818-0d40-445e-a3c0-0f46723a25e22023-11-29Warnings, Adverse reactionsExact identifier
rxcui: 2471878

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
36c5c818-0d40-445e-a3c0-0f46723a25e2Wynzora 0.005 % / 0.064 % Topical Cream [PSN] · betamethasone dipropionate 0.64 MG/ML / calcipotriene 0.05 MG/ML Topical Cream [Wynzora] [SBD] · Wynzora (calcipotriene 0.005 % / betamethasone dipropionate 0.064 % ) Topical Cream [SY]36These highlights do not include all the information needed to use WYNZORA Cream safely and effectively. See full prescribing information for WYNZORA Cream. WYNZORA ® (calcipotriene and betamethasone dipropionate) cream, for topical use Initial U.S. Approval: 202020231129