FDA.reportPublic FDA data

FDA label 4a4c3bfa-32ef-c0dd-e063-6394a90ab15c

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
3952c0c0-3173-55ed-e063-6294a90ad94f
SPL ID
4a4c3bfa-32ef-c0dd-e063-6394a90ab15c
Version
2
Effective date
2026-02-08
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 05:19:01

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.