Home FDA labels 1d75dc5e-3f67-d0c3-e063-6294a90aac2b Fluocinonide openFDA label record# This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)
Brand name Fluocinonide
Generic name FLUOCINONIDE
Manufacturer NuCare Pharmaceuticals,Inc.
Product type HUMAN PRESCRIPTION DRUG
SPL set ID a8eefd01-340e-5eef-e053-2a95a90a802c
SPL ID 1d75dc5e-3f67-d0c3-e063-6294a90aac2b
Version 3
Effective date 2024-07-17
Source export date 2026-09-28
Source partition 11
Source file https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 06:15:20 Harmonized routes table Harmonized routes TOPICAL
Harmonized identifier links# Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
Harmonized identifiers page 1 of 1 · 12 matching rows.
Adverse reactions cross-check# openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Adverse reactions sections page 1 of 1 · 2 matching rows.
adverse reactions ADVERSE REACTIONS The following local adverse reactions are reported infrequently with topical corticosteroids, but may occur more frequently with the use of occlusive dressings. These reactions are listed in an approximate decreasing order of occurrence: Burning Perioral dermatitis Itching Allergic contact dermatitis Irritation Maceration of the skin Dryness Secondary infection Folliculitis Skin atrophy Hypertrichosis Striae Acneiform eruptions Miliaria Hypopigmentation
adverse reactions table <table><col width="21%"/><col width="27%"/><tbody><tr><td styleCode=" Botrule Toprule Lrule " valign="top"><paragraph>Burning</paragraph></td><td styleCode=" Botrule Toprule Lrule " valign="top"><paragraph>Perioral dermatitis</paragraph></td></tr><tr><td styleCode=" Botrule Lrule " valign="top"><paragraph>Itching</paragraph></td><td styleCode=" Botrule Lrule " valign="top"><paragraph>Allergic contact dermatitis</paragraph></td></tr><tr><td styleCode=" Botrule Lrule " valign="top"><paragraph>Irritation</paragraph></td><td styleCode=" Botrule Lrule " valign="top"><paragraph>Maceration of the skin</paragraph></td></tr><tr><td styleCode=" Botrule Lrule " valign="top"><paragraph>Dryness</paragraph></td><td styleCode=" Botrule Lrule " valign="top"><paragraph>Secondary infection</paragraph></td></tr><tr><td styleCode=" Botrule Lrule " valign="top"><paragraph>Folliculitis</paragraph></td><td styleCode=" Botrule Lrule " valign="top"><paragraph>Skin atrophy</paragraph></td></tr><tr><td styleCode=" Botrule Lrule " valign="top"><paragraph>Hypertrichosis</paragraph></td><td styleCode=" Botrule Lrule " valign="top"><paragraph>Striae</paragraph></td></tr><tr><td styleCode=" Botrule Lrule " valign="top"><paragraph>Acneiform eruptions</paragraph></td><td styleCode=" Botrule Lrule " valign="top"><paragraph>Miliaria</paragraph></td></tr><tr><td styleCode=" Botrule Lrule " valign="top"><paragraph>Hypopigmentation</paragraph></td><td styleCode=" Botrule Lrule " valign="top"/></tr></tbody></table>
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.