FDA label 51ead28a-8e79-69c1-e063-6294a90ad1a3

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
3432c4a6-3e48-db91-e063-6394a90a28ee
SPL ID
51ead28a-8e79-69c1-e063-6294a90ad1a3
Version
2
Effective date
2026-05-16
Source export date
2026-10-12
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:17:21

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 1.Do not use if you are allergic to the ingredients. 2.Ask a doctor before use if you have Heart disease、High blood pressure、Thyroid disease、Diabetes、Trouble urinating due to enlarged prostate gland 3.When using this product ·Do not exceed recommended dosage ·After continuous use for 3 days, please stop using for 1 day, please use as instructed.Do not use without nasal congestion.Frequent or prolonged use may cause nasalcongestion to recur or worsen. ·Temporary discomfort such as burning, stinging, sneezing, or increased nasal discharge may occur. ·Use of this container by more than one person may spread infection.

Reported adverse events (FAERS/openFDA)#

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