FDA.reportPublic FDA data

FDA label da69902d-5573-4427-aa22-8b3c19cdfce3

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
cfa86231-1405-4562-9af5-4da2fe245c2a
SPL ID
da69902d-5573-4427-aa22-8b3c19cdfce3
Version
3
Effective date
2016-12-07
Source export date
2026-08-08
Source partition
13
Source file
https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-08-08/2ef638b6b5a68e854d11a3945e1b1aa8d0e7f812a9d69af10df01eecf2e189d0/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
b39f3b00ad50d2e1b32aaf429248c6081e8799b35bce715b4fccb8cfa1ac4546
Import run
20260810T161303Z
Imported at
2026-08-10 18:02:55

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 When using this product • do not touch tip of container to any surface to avoid contamination • replace cap after each use • do not use if solution changes color or becomes cloudy • remove contact lenses before using Stop use and ask a doctor if you feel eye pain changes in vision occur redness or irritation of the eyes lasts condition worsens or lasts more than 72 hours