FDA.reportPublic FDA data

FDA label 3cb9857f-529c-ad6c-e063-6294a90aa418

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
3cb9857f-529b-ad6c-e063-6294a90aa418
SPL ID
3cb9857f-529c-ad6c-e063-6294a90aa418
Version
1
Effective date
2025-08-18
Source export date
2026-09-28
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:26:53

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 If this product changes color or becomes cloudy If you are sensitive to any ingredient in this product. Do not use if imprinted seal around cap is broken or bottle is damaged When using this product Make sure the tip of container does not touch any surface to avoid contamination. Replace cap after each use Stop use and ask a doctor if you experience any of the following: Eye pain, changes in vision, continued redness or irritation of the eye Condition worsens or persists for more than 72 hours 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.