FDA.reportPublic FDA data

FDA label 4f11f1ce-389e-2523-e063-6294a90aba50

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
4f11f1ce-389d-2523-e063-6294a90aba50
SPL ID
4f11f1ce-389e-2523-e063-6294a90aba50
Version
1
Effective date
2026-04-09
Source export date
2026-11-06
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/2026-11-06/97001096994db9ca8cee114e6c3bb5298d3c573158ffc1ab8692d82e76a3eb40/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 06:56:28

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 inhalation use only. Do not ingest or apply to skin. Avoid direct contact with eyes. If contact occurs, rinse thoroughly with water for 15 minutes. Use only as directed. Misuse may be harmful. Use in a well-ventilated area. Do not use in enclosed spaces. Prolonged exposure may cause irritation. Discontinue use if discomfort occurs. Possible side effects include nasal irritation, coughing, or shortness of breath. If symptoms persist, discontinue use and consult a doctor.

Reported adverse events (FAERS/openFDA)#

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