FDA.reportPublic FDA data

FDA label 7d9d8744-e312-483a-bcd9-6894e61114cb

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
a9f844af-6887-4496-8c64-721357a4a5bb
SPL ID
7d9d8744-e312-483a-bcd9-6894e61114cb
Version
2
Effective date
2018-08-03
Source export date
2026-08-01
Source partition
1
Source file
https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-08-01/0689a4374f1490600b5244071db3b04bd3bbc29ceda7a856edb8225323adf20a/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:00:27

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 • replace cap after use • do not touch tip of container to any surface to avoid contamination 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