FDA label 06be0fe1-cc2d-4ec7-8e3f-5af027e1f7ae

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
dba096d3-228b-4b74-83cc-9cb2c70d39f9
SPL ID
06be0fe1-cc2d-4ec7-8e3f-5af027e1f7ae
Version
3
Effective date
2016-08-18
Source export date
2026-09-28
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:21:34

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: If nasal symptoms do not improve within 7 days or are accompanied by a fever, consult a doctor. Do not take this product for pain for more than 10 days (adult) or 5 days (children) unless directed by a doctor. If pain persists or gets worse, if new symptoms occur, or if redness or swelling is present, consult a doctor becasue these could be signs of a serious condition. If pregnant or breast-feeding, ask a healthcare professional before use.

Reported adverse events (FAERS/openFDA)#

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