FDA label a31b5d08-e78b-4965-8a70-d2e5f303dfd7

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
38e7481f-cba1-489b-a0d6-1847e5d8c360
SPL ID
a31b5d08-e78b-4965-8a70-d2e5f303dfd7
Version
1
Effective date
2013-10-25
Source export date
2026-08-01
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/2026-08-01/4d7120b2932458966cd5c2f0e3ab49319f616f09498d059c9ff283a8dac64565/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:12:16

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 have been reported with corticosteroid suppositories: 1. Burning 2. Itching 3. Irritation 4. Dryness 5. Folliculitis 6. Hypopigmentation 7. Allergic Contact Dermatitis 8. Secondary Infection

adverse reactions table

<table width="75%" styleCode="Noautorules"> <col width="50%" align="left" valign="top"/> <col width="50%" align="left" valign="top"/> <tbody> <tr> <td> <list listType="unordered"> <item> <caption>1.</caption>Burning</item> <item> <caption>2.</caption>Itching</item> <item> <caption>3.</caption>Irritation</item> <item> <caption>4.</caption>Dryness</item> </list> </td> <td> <list listType="unordered"> <item> <caption>5.</caption>Folliculitis</item> <item> <caption>6.</caption>Hypopigmentation</item> <item> <caption>7.</caption>Allergic Contact Dermatitis</item> <item> <caption>8.</caption>Secondary Infection</item> </list> </td> </tr> </tbody> </table>