FDA label 1d4dfd92-123a-a873-e063-6394a90abb8d

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
74af00f8-e861-6ce3-e053-2991aa0ad576
SPL ID
1d4dfd92-123a-a873-e063-6394a90abb8d
Version
3
Effective date
2024-07-15
Source export date
2026-09-28
Source partition
1
Source file
https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/9c7783846d422acb0c9e59457606951c785a7d28cc631c8cc4839d0dc7c55f39/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:14:11

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 width="100%"><col width="21%"/><col width="27%"/><tbody><tr><td styleCode="Botrule Lrule Toprule " valign="top"><paragraph>Burning</paragraph></td><td styleCode="Botrule Lrule Toprule " valign="top"><paragraph>Perioral dermatitis</paragraph></td></tr><tr><td styleCode="Lrule Botrule " valign="top"><paragraph>Itching</paragraph></td><td styleCode="Lrule Botrule " valign="top"><paragraph>Allergic contact dermatitis</paragraph></td></tr><tr><td styleCode="Lrule Botrule " valign="top"><paragraph>Irritation</paragraph></td><td styleCode="Lrule Botrule " valign="top"><paragraph>Maceration of the skin</paragraph></td></tr><tr><td styleCode="Lrule Botrule " valign="top"><paragraph>Dryness</paragraph></td><td styleCode="Lrule Botrule " valign="top"><paragraph>Secondary infection</paragraph></td></tr><tr><td styleCode="Lrule Botrule " valign="top"><paragraph>Folliculitis</paragraph></td><td styleCode="Lrule Botrule " valign="top"><paragraph>Skin atrophy</paragraph></td></tr><tr><td styleCode="Lrule Botrule " valign="top"><paragraph>Hypertrichosis</paragraph></td><td styleCode="Lrule Botrule " valign="top"><paragraph>Striae</paragraph></td></tr><tr><td styleCode="Lrule Botrule " valign="top"><paragraph>Acneiform eruptions</paragraph></td><td styleCode="Lrule Botrule " 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.