warnings
WARNINGS For external use only. Not for ophthalmic use. Product could harm small children if chewed or swallowed. Individual tubes are NOT child resistant. Keep product and cleansing wipes out of the reach of children.
FDA label 0810c1d7-144f-4019-9c0d-c23015e3bf03
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
- SPL set ID
- 29e01360-5b59-4f8a-a2f4-bdabbd7dbcc5
- SPL ID
- 0810c1d7-144f-4019-9c0d-c23015e3bf03
- Version
- 2
- Effective date
- 2017-02-16
- Source export date
- 2026-10-12
- Source partition
- 8
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:07:35
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| spl id | 0810c1d7-144f-4019-9c0d-c23015e3bf03 | id | |
| spl set id | 29e01360-5b59-4f8a-a2f4-bdabbd7dbcc5 | set_id |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
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 Dryness Perioral dermatitis Skin atrophy Itching Folliculitis Hypertrichosis Allergic contact dermatitis Striae Irritation Acneiform eruptions Maceration of the skin Miliaria Hypopigmentation Secondary infection
adverse reactions table
<table width="90%"> <col width="15%" align="left" valign="top"/> <col width="30%" align="left" valign="top"/> <col width="35%" align="left" valign="top"/> <col width="20%" align="left" valign="top"/> <tbody> <tr styleCode="TopRule"> <td>Burning</td> <td>Dryness</td> <td>Perioral dermatitis</td> <td>Skin atrophy</td> </tr> <tr> <td>Itching</td> <td>Folliculitis Hypertrichosis</td> <td>Allergic contact dermatitis</td> <td>Striae</td> </tr> <tr> <td>Irritation</td> <td>Acneiform eruptions</td> <td>Maceration of the skin</td> <td>Miliaria</td> </tr> <tr styleCode="BotRule"> <td> </td> <td>Hypopigmentation</td> <td>Secondary infection</td> <td> </td> </tr> </tbody> </table>
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.