FDA label 445c3379-d0e0-7420-e063-6294a90a574a

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
adb355fa-8bc4-48f5-90ab-098d95dcfd1a
SPL ID
445c3379-d0e0-7420-e063-6294a90a574a
Version
2
Effective date
2025-11-24
Source export date
2026-09-28
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:18:40

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings: For external use only . Avoid contact with eyes, mucous membranes, wounds, damaged or irritated skin. If pregnant or breast-feeding, ask a health professional before use. Nursing mothers should not apply to breast area. Keep out of reach of children. Stop use and ask a doctor if : •symptoms worsen or do not improve within 3 days •skin irritation, redness or rash occurs.

Reported adverse events (FAERS/openFDA)#

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