FDA label 71607b3f-aac5-4d9f-bc7b-b968f7b1baff

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
ecb22eaf-4142-471c-95c6-a1b54eca8b7a
SPL ID
71607b3f-aac5-4d9f-bc7b-b968f7b1baff
Version
1
Effective date
2016-03-31
Source export date
2026-11-06
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/2026-11-06/bbdc0a42bf44145a63c3752991067bece7e2a518be6cc14943d33c4987faa012/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:09:32

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: When using this product DO NOT EXCEED RECOMMENDED DOSAGE. Temporary BURNING, STINGING, SNEEZING, OR AN INCREASED IN NASAL DISCHARGE may occur. 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.

Reported adverse events (FAERS/openFDA)#

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