FDA label 0075774d-9b1f-7e25-e063-6394a90a0fc1

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
cc994062-9f2e-8be3-e053-2995a90a3f8b
SPL ID
0075774d-9b1f-7e25-e063-6394a90a0fc1
Version
2
Effective date
2023-07-14
Source export date
2026-09-28
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:39:03

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 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 cellspacing="0" cellpadding="0" border="0" width="100%"><col width="26.42%"/><col width="42.38%"/><col width="31.22%"/><tbody><tr styleCode="Botrule"><td align="justify" styleCode="Lrule Rrule" valign="top">Burning </td><td align="justify" styleCode="Rrule" valign="top">Hypertrichosis </td><td align="justify" styleCode="Rrule" valign="top">Maceration of the skin </td></tr><tr styleCode="Botrule"><td align="justify" styleCode="Lrule Rrule" valign="top">Itching </td><td align="justify" styleCode="Rrule" valign="top">Acneiform eruptions </td><td align="justify" styleCode="Rrule" valign="top">Secondary infection </td></tr><tr styleCode="Botrule"><td align="justify" styleCode="Lrule Rrule" valign="top">Irritation </td><td align="justify" styleCode="Rrule" valign="top">Hypopigmentation </td><td align="justify" styleCode="Rrule" valign="top">Skin atrophy </td></tr><tr styleCode="Botrule"><td align="justify" styleCode="Lrule Rrule" valign="top">Dryness </td><td align="justify" styleCode="Rrule" valign="top">Perioral dermatitis </td><td align="justify" styleCode="Rrule" valign="top">Striae </td></tr><tr><td align="justify" styleCode="Lrule Rrule" valign="top">Folliculitis </td><td align="justify" styleCode="Rrule" valign="top">Allergic contact dermatitis </td><td align="justify" styleCode="Rrule" valign="top">Miliaria </td></tr></tbody></table>

Reported adverse events (FAERS/openFDA)#

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