FDA label 36d08534-ac8d-5152-e063-6294a90ae129

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
36ceef42-c3ea-7302-e063-6394a90a94da
SPL ID
36d08534-ac8d-5152-e063-6294a90ae129
Version
2
Effective date
2025-06-05
Source export date
2026-09-28
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/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:07:40

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. Do not ingest or apply to skin. Avoid direct contact with eyes. lfcontact occurs, rinsethoroughly 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 useif discomfort occurs. Possible side effects include nasal imitation, coughing, orshortness ofbreath. lfsymptoms persist, discontinue useand consult a doctor.

Reported adverse events (FAERS/openFDA)#

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