FDA label e211ff51-e8bd-4ffa-9d57-afa03062a56e

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
cd959b0a-0ca2-48a0-a4ba-984ac4c130f6
SPL ID
e211ff51-e8bd-4ffa-9d57-afa03062a56e
Version
1
Effective date
2019-01-29
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 05:30:39

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. • This product may cause temporary discomfort such as burning, stinging, sneezing or an increase in nasal discharge. • ​The use of this container by more than one person may spread infection. • For your safety there is a full body seal over bottle printed "sealed for your protection." Do not use if seal is broken or missing. • ​If pregnant or breast-feeding, ​ask a health care 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.