FDA.reportPublic FDA data

alitretinoin 0.1 % Topical Gel

RxCUI
313847
RxNorm name
alitretinoin 0.1 % Topical Gel
Display name
alitretinoin 0.1 % Topical Gel
Full name
alitretinoin 0.1 % Topical Gel
Term type
PSN
Status
DailyMed mapping
Updated
2026-06-04 23:38:56

RxNav Current And Historical NDCs#

RxNav current and historical NDC rows page 1 of 1 · 0 matching rows.

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
PANRETINALITRETINOINAdvanz Pharma (US) Corp.49c16717-7d86-4257-80c9-baa1417e55552025-11-25Warnings, Adverse reactionsExact identifier
rxcui: 313847

DailyMed RxNorm Mappings#

unique DailyMed labels mapped to this RxNorm concept page 1 of 1 · 2 matching rows.

Set ID, RxNorm mappings, Terms table
Set IDRxNorm mappingsTermsSPL versionLabelEffective
49c16717-7d86-4257-80c9-baa1417e5555alitretinoin 0.1 % Topical Gel [PSN] · alitretinoin 0.001 MG/MG Topical Gel [SCD] · alitretinoin 0.1 % Topical Gel [SY]36These highlights do not include all the information needed to use PANRETIN GEL safely and effectively. See full prescribing information for PANRETIN GEL. PANRETIN GEL (alitretinoin) 0.1%, for topical use Initial U.S. Approval: 199920251125
9cf04dad-e312-4b8f-a297-1e002d43e151alitretinoin 0.1 % Topical Gel [PSN] · alitretinoin 0.001 MG/MG Topical Gel [SCD] · alitretinoin 0.1 % Topical Gel [SY]31Panretin® (alitretinoin) gel 0.1% (For topical use only)20061006