Home FDA labels 326b872f-bb48-590b-e054-00144ff8d46c FDA label 326b872f-bb48-590b-e054-00144ff8d46c openFDA label record# This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
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SPL set ID 58644a25-eb04-4571-950e-269b43c58581
SPL ID 326b872f-bb48-590b-e054-00144ff8d46c
Version 3
Effective date 2016-05-09
Source export date 2026-09-28
Source partition 12
Source file https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 06:22:17
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adverse reactions ADVERSE REACTIONS The following local adverse reactions have been reported infrequently with topical corticosteroids. They may occur more frequently with the use of occlusive dressings, especially with higher potency corticosteroids. These reactions are listed in an approximate decreasing order of occurrence: burning, itching, irritation, dryness, folliculitis, acneiform eruptions, hypopigmentation, perioral dermatitis, allergic contact dermatitis, secondary infection, skin atrophy, striae, and miliaria. One peanut sensitive child experienced a flare of his atopic dermatitis after 5 days of twice daily treatment with fluocinolone acetonide topical oil, 0.01%. A post marketing (open-label) safety study was conducted in 58 children to evaluate the local safety of fluocinolone acetonide topical oil, 0.01% when applied twice daily for 4 weeks to the face in children (2 to 12 years) with moderate to severe atopic dermatitis (see Table of Incidence of Adverse Events). Incidence of Adverse Events (%) N=58 Adverse Event (AE) The number of individual adverse events reported does not necessarily reflect the number of individual subjects, since one subject could have multiple reporting of an adverse event. # of patients (%) Day 14 Day 28 End of Treatment Day 56 Four Weeks Post Treatment Any AE 15 (25.9) 6 (10.3) 7 (12.1) 7 (12.1) Telangiectasia 5 (8.6) 3 (5.2) 4 (6.9) 2 (3.5) Erythema 3 (5.2) 3 (5.2) Itching 3 (5.2) 3 (5.2) Irritation 3 (5.2) 3 (5.2) Burning 3 (5.2) 3 (5.2) Hypopigmentation 2 (3.5) 2 (3.5) Shiny Skin 1 (1.7) 1 (1.7) Secondary atopic dermatitis 1 (1.7) 1 (1.7) Papules and pustules 1 (1.7) 1 (1.7) Keratosis pilaris 1 (1.7) 1 (1.7) Folliculitis 1 (1.7) 1 (1.7) Facial herpes simplex 1 (1.7) 1 (1.7) Acneiform eruption 1 (1.7) 1 (1.7) Ear infection 1 (1.7) 1 (1.7)
adverse reactions table <table width="90%" ID="ccfc62fb-240e-495b-aa21-fab2afe94824"> <caption/> <col width="40%" align="left"/> <col width="15%" align="center"/> <col width="15%" align="center"/> <col width="15%" valign="top" align="center"/> <col width="15%" valign="top" align="center"/> <tbody> <tr styleCode="Botrule"> <td align="center" colspan="5" styleCode="Lrule Rrule"> <content styleCode="bold">Incidence of Adverse Events (%)</content> N=58 </td> </tr> <tr styleCode="Botrule"> <td styleCode="Lrule">Adverse Event (AE) <footnote ID="K622">The number of individual adverse events reported does not necessarily reflect the number of individual subjects, since one subject could have multiple reporting of an adverse event.</footnote> </td> <td styleCode="Lrule"># of patients (%) </td> <td styleCode="Lrule">Day 14</td> <td styleCode="Lrule">Day 28 <footnote ID="K635">End of Treatment</footnote> </td> <td styleCode="Lrule Rrule">Day 56 <footnote ID="K640">Four Weeks Post Treatment</footnote> </td> </tr> <tr styleCode="Botrule"> <td styleCode="Lrule">Any AE</td> <td styleCode="Lrule">15 (25.9)</td> <td styleCode="Lrule">6 (10.3)</td> <td styleCode="Lrule">7 (12.1)</td> <td styleCode="Lrule Rrule">7 (12.1)</td> </tr> <tr styleCode="Botrule"> <td styleCode="Lrule">Telangiectasia</td> <td styleCode="Lrule">5 (8.6)</td> <td styleCode="Lrule">3 (5.2)</td> <td styleCode="Lrule">4 (6.9)</td> <td styleCode="Lrule Rrule">2 (3.5)</td> </tr> <tr styleCode="Botrule"> <td styleCode="Lrule">Erythema</td> <td styleCode="Lrule">3 (5.2)</td> <td styleCode="Lrule"/> <td styleCode="Lrule"/> <td styleCode="Lrule Rrule">3 (5.2)</td> </tr> <tr styleCode="Botrule"> <td styleCode="Lrule">Itching</td> <td styleCode="Lrule">3 (5.2)</td> <td styleCode="Lrule"/> <td styleCode="Lrule"/> <td styleCode="Lrule Rrule">3 (5.2)</td> </tr> <tr styleCode="Botrule"> <td styleCode="Lrule">Irritation</td> <td styleCode="Lrule">3 (5.2)</td> <td styleCode="Lrule"/> <td styleCode="Lrule"/> <td styleCode="Lrule Rrule">3 (5.2)</td> </tr> <tr styleCode="Botrule"> <td styleCode="Lrule">Burning</td> <td styleCode="Lrule">3 (5.2)</td> <td styleCode="Lrule"/> <td styleCode="Lrule"/> <td styleCode="Lrule Rrule">3 (5.2)</td> </tr> <tr styleCode="Botrule"> <td styleCode="Lrule">Hypopigmentation</td> <td styleCode="Lrule">2 (3.5)</td> <td styleCode="Lrule">2 (3.5)</td> <td styleCode="Lrule"/> <td styleCode="Lrule Rrule"/> </tr> <tr styleCode="Botrule"> <td styleCode="Lrule">Shiny Skin</td> <td styleCode="Lrule">1 (1.7)</td> <td styleCode="Lrule"/> <td styleCode="Lrule">1 (1.7)</td> <td styleCode="Lrule Rrule"/> </tr> <tr styleCode="Botrule"> <td styleCode="Lrule">Secondary atopic dermatitis</td> <td styleCode="Lrule">1 (1.7)</td> <td styleCode="Lrule"/> <td styleCode="Lrule"/> <td styleCode="Lrule Rrule">1 (1.7)</td> </tr> <tr styleCode="Botrule"> <td styleCode="Lrule">Papules and pustules</td> <td styleCode="Lrule">1 (1.7)</td> <td styleCode="Lrule"/> <td styleCode="Lrule"/> <td styleCode="Lrule Rrule">1 (1.7)</td> </tr> <tr styleCode="Botrule"> <td styleCode="Lrule">Keratosis pilaris</td> <td styleCode="Lrule">1 (1.7)</td> <td styleCode="Lrule"/> <td styleCode="Lrule"/> <td styleCode="Lrule Rrule">1 (1.7)</td> </tr> <tr styleCode="Botrule"> <td styleCode="Lrule">Folliculitis</td> <td styleCode="Lrule">1 (1.7)</td> <td styleCode="Lrule"/> <td styleCode="Lrule">1 (1.7)</td> <td styleCode="Lrule Rrule"/> </tr> <tr styleCode="Botrule"> <td styleCode="Lrule">Facial herpes simplex</td> <td styleCode="Lrule">1 (1.7)</td> <td styleCode="Lrule">1 (1.7)</td> <td styleCode="Lrule"/> <td styleCode="Lrule Rrule"/> </tr> <tr styleCode="Botrule"> <td styleCode="Lrule">Acneiform eruption</td> <td styleCode="Lrule">1 (1.7)</td> <td styleCode="Lrule"/> <td styleCode="Lrule">1 (1.7)</td> <td styleCode="Lrule Rrule"/> </tr> <tr> <td styleCode="Lrule">Ear infection</td> <td styleCode="Lrule">1 (1.7)</td> <td styleCode="Lrule"/> <td styleCode="Lrule">1 (1.7)</td> <td styleCode="Lrule Rrule"/> </tr> </tbody> </table>
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.