Home FDA labels 9922be09-ec29-44db-a22b-12e98ba5007d TRIAMCINOLONE ACETONIDE 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)
Brand name TRIAMCINOLONE ACETONIDE
Generic name TRIAMCINOLONE ACETONIDE
Manufacturer QUAGEN PHARMACEUTICALS LLC
Product type HUMAN PRESCRIPTION DRUG
SPL set ID 4c6ff738-60a3-4339-8e94-26fb9df65841
SPL ID 9922be09-ec29-44db-a22b-12e98ba5007d
Version 4
Effective date 2025-07-22
Source export date 2026-09-28
Source partition 10
Source file https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 06:06:08 Harmonized routes table Harmonized routes TOPICAL
Harmonized identifier links# Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
Harmonized identifiers page 1 of 1 · 16 matching rows.
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="50%" border="1" cellspacing="5"><caption/><tbody><tr><td styleCode="Rrule"> Burning</td><td> Perioral dermatitis</td></tr><tr><td styleCode="Rrule"> Itching</td><td> Allergic contact dermatitis</td></tr><tr><td styleCode="Rrule"> Irritation</td><td> Maceration of the skin</td></tr><tr><td styleCode="Rrule"> Dryness</td><td> Secondary infection</td></tr><tr><td styleCode="Rrule"> Folliculitis</td><td> Skin Atrophy</td></tr><tr><td styleCode="Rrule"> Hypertrichosis</td><td> Striae</td></tr><tr><td styleCode="Rrule"> Acneiform eruptions</td><td> Miliaria</td></tr><tr><td styleCode="Rrule"> Hypopigmentation</td><td/></tr></tbody></table>
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.