FDA.reportPublic FDA data

FDA label 27dc2889-79cf-8a37-e063-6394a90aeee2

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
d44e8198-8ba1-46ee-be88-0228368b7640
SPL ID
27dc2889-79cf-8a37-e063-6394a90aeee2
Version
4
Effective date
2024-11-26
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 05:20:47

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: For external use only Do not use Except under the advice and supervision of a doctor When using this product It may cause temporary burning and irritation Replace cap after use To avoid contamination, do not touch top of container to any surface Stop use and ask a doctor if Condition worsens or persists for more than 72 hours You experience eye pain, changes in vision, continued redness or irritation of the eye 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.