Home FDA labels 46b8a0e4-33c6-3f8b-e063-6294a90a8740 FDA label 46b8a0e4-33c6-3f8b-e063-6294a90a8740 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)
SPL set ID f96f4f15-9b99-446e-8e58-6a99ade5ba77
SPL ID 46b8a0e4-33c6-3f8b-e063-6294a90a8740
Version 3
Effective date 2025-12-24
Source export date 2026-09-28
Source partition 10
Source file https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 06:05:45 Harmonized identifier links# Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
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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 Hypertrichosis Maceration of the Skin Itching Acneiform Eruptions Secondary Infection Irritation Hypopigmentation Skin Atrophy Dryness Perioral Dermatitis Striae Folliculitis Allergic Contact Dermatitis Miliaria
adverse reactions table <table width="80%" styleCode="Noautorules"><col width="30%" align="left" valign="top"/><col width="35%" align="left" valign="top"/><col width="35%" align="left" valign="top"/><tbody><tr><td>Burning</td><td>Hypertrichosis</td><td>Maceration of the Skin</td></tr><tr><td>Itching</td><td>Acneiform Eruptions</td><td>Secondary Infection</td></tr><tr><td>Irritation</td><td>Hypopigmentation</td><td>Skin Atrophy</td></tr><tr><td>Dryness</td><td>Perioral Dermatitis</td><td>Striae</td></tr><tr><td>Folliculitis</td><td>Allergic Contact Dermatitis</td><td>Miliaria</td></tr></tbody></table>
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.