FDA.reportPublic FDA data

FDA label 3e7d9782-4551-9f08-e063-6294a90a4f35

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
38c57576-e2c1-c447-e063-6394a90a62ae
SPL ID
3e7d9782-4551-9f08-e063-6294a90a4f35
Version
4
Effective date
2025-09-10
Source export date
2026-09-28
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:18:23

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

ForinHalAtion use only. Do notingest or apply to skin. Avoid direct contact with eyes. lfcontact occurs, rinse thoroughly with water for l5 minutes. Use only as directed. Misuse may be harmful. Use in a well-ventilated area. Donot usein enclosed spaces. Prolonged exposure may cause irritation. Discontinue use if discomfort occurs. Possible side effectsinclude nasaliritation, coughing, or shortness of breath.lf symptoms persist, discontinue use and consult a doctor.

Reported adverse events (FAERS/openFDA)#

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