FDA label 1d4f69e3-7f14-4549-e063-6294a90a36b9

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
2949cac2-8597-49e8-a64d-6a97060faad7
SPL ID
1d4f69e3-7f14-4549-e063-6294a90a36b9
Version
3
Effective date
2024-07-15
Source export date
2026-10-12
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/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:40:34

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: DO NOT EXCEED RECOMMENDED DOSAGE. THIS PRODUCT MAY CAUSE TEMPORARY DISCOMFORT SUCH AS BURNING, STINGING, SNEEZING, OR AN INCREASED IN NASAL DISCHARGE. THE USE OF THIS CONTAINER BY MORE THAN ONE PERSON MAY SPREAD INFECTION. DO NOT USE THIS PRODUCT FOR MORE THAN 7 DAY. USE ONLY AS DISRECTED. FREQUENT OR PROLONGED USE MAY CAUSE NASAL CONGESTION TO RECUR OR WORSEN. IF SYMPTOMS PERSIST, CONSULT A DOCTOR.

Reported adverse events (FAERS/openFDA)#

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