FDA.reportPublic FDA data

FDA label 5856c130-4114-6037-e063-6294a90ab284

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
42699816-1ae2-cfea-e063-6394a90aec1f
SPL ID
5856c130-4114-6037-e063-6294a90ab284
Version
5
Effective date
2026-08-05
Source export date
2026-10-12
Source partition
2
Source file
https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/4760f38f2bcb10aa20ddbadb42b270d31e9f2a8024440d3af3dec8d11feb92ec/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:28:18

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 external use only. Do not use • If you have respiratory conditions such as asthma or emphysema unless directed by a doctor When using this product • Avoid prolonged or repeated inhalation • Do not apply directly to the nostrils • Avoid contact with eyes and skin Stop use and ask a doctor if • Symptoms persist or worsen • Irritation or discomfort occurs Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center right away (1-800-222-1222).

Reported adverse events (FAERS/openFDA)#

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