ALITRETINOIN - Food and Drug Administration

Manufacturer: Food and Drug Administration
Effective date: 2014-05-08
Label type: Indexing - Product Concept
Version: 1
Source: full-release
Hydrated at: 2026-06-05 00:14:12

Label at a glance#

ProductALITRETINOIN

Active ingredientALITRETINOIN

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 1 matching rows.

ALITRETINOIN

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 1 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALITRETINOIN	1UA8E65KDZ	ACTIB

Source Document#

Source XML

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
PANRETIN	ALITRETINOIN	Advanz Pharma (US) Corp.	49c16717-7d86-4257-80c9-baa1417e5555	2025-11-25	Warnings, Adverse reactions	Name fallback generic name: ALITRETINOIN

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.