FDA label 7fa9cf7b-a160-9c4a-e053-2991aa0a0a9d

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
e8d8f870-b297-44d0-9555-5130ff816b7f
SPL ID
7fa9cf7b-a160-9c4a-e053-2991aa0a0a9d
Version
2
Effective date
2019-01-17
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 05:29:07

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. Do not use with any other products containing decongestants . Ask a doctor before use if the child has heart disease high blood pressure thyroid disease diabetes When using this product Temporary discomfort such as burning, stinging, sneezing or an increase in nasal discharge may occur. The use of this dispenser by more than one person may spread infection. Do not use for more than 3 days Use only as directed. Frequent or prolonged use may cause nasal congestion to recur or worsen. Stop use and ask a doctor if symptoms persist. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Reported adverse events (FAERS/openFDA)#

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