FDA label 1ab666d4-ad64-276b-e063-6394a90a1ce3

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
7973733b-d48c-1e6b-e053-2991aa0afb47
SPL ID
1ab666d4-ad64-276b-e063-6394a90a1ce3
Version
6
Effective date
2024-06-12
Source export date
2026-10-12
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:31:12

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="60%"><col align="left" valign="top" width="45%"/><col align="left" valign="top" width="55%"/><tbody><tr styleCode="Botrule"><td styleCode="Lrule Rrule">Burning</td><td styleCode="Rrule">Perioral dermatitis</td></tr><tr styleCode="Botrule"><td styleCode="Lrule Rrule">Itching</td><td styleCode="Rrule">Allergic contact dermatitis</td></tr><tr styleCode="Botrule"><td styleCode="Lrule Rrule">Irritation</td><td styleCode="Rrule">Maceration of the skin</td></tr><tr styleCode="Botrule"><td styleCode="Lrule Rrule">Dryness</td><td styleCode="Rrule">Secondary infection</td></tr><tr styleCode="Botrule"><td styleCode="Lrule Rrule">Folliculitis</td><td styleCode="Rrule">Skin atrophy</td></tr><tr styleCode="Botrule"><td styleCode="Lrule Rrule">Hypertrichosis</td><td styleCode="Rrule">Striae</td></tr><tr styleCode="Botrule"><td styleCode="Lrule Rrule">Acneiform eruptions</td><td styleCode="Rrule">Miliaria</td></tr><tr><td styleCode="Lrule Rrule">Hypopigmentation</td><td styleCode="Rrule"/></tr></tbody></table>

Reported adverse events (FAERS/openFDA)#

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