FDA.reportPublic FDA data

FDA label 4a602306-dae8-d05b-e063-6294a90af7e0

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
33a54465-324a-9f07-e063-6394a90a6040
SPL ID
4a602306-dae8-d05b-e063-6294a90af7e0
Version
3
Effective date
2026-02-09
Source export date
2026-10-12
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:17:52

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.