FDA label 781ec1ad-a216-5df4-e053-2991aa0a6341

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
b573c05d-b783-4558-87ec-dd5061131f57
SPL ID
781ec1ad-a216-5df4-e053-2991aa0a6341
Version
8
Effective date
2017-12-31
Source export date
2026-09-28
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:29:59

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 nasal use only Do not use if you have an allergy or hypersensitivity to the components of the formula or if you have had a prior reaction to this product Ask a doctor before use if you are under a doctor's care for any serious condition, such as asthma taking any other drug When using this product do not exceed recommended dosage temporary discomfort such as burning, stinging, sneezing, or an increase in nasal discharge may occur avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water use of this container by more than one person may spread infection Stop use and ask a doctor if symptoms persist, worsen, or if new symptoms occur. If pregnant or breastfeeding , as a health professional before use. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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