FDA label 3e7d9eff-dd7a-668e-e063-6394a90a404f

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
38601f38-09ef-9bb2-e063-6294a90a83d6
SPL ID
3e7d9eff-dd7a-668e-e063-6394a90a404f
Version
4
Effective date
2025-09-10
Source export date
2026-11-06
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/b0d9ca61dc485ebaf55e14a76d7d677668e40ef1e1978cdbcc4d73d58eba0b99/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:46:23

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

For inHalAtion use only. Avoid direct contact with eyes.lfcontact occurs,rinse thoroughly with water fori5 minutes.Use only as directed. Misuse may be harmful. Use in a well-ventilated area.Do notuse in enclosedspaces Prolonged exposure maycause irritation.Discantinue useifdiscomfort occurs. Possible side effectsinclude nasallritation,coughing.or shortness of breath.lfsymptoms persist, discontinue use and consulta doctor

Reported adverse events (FAERS/openFDA)#

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