FDA label 32f41ea8-ea6a-4526-b0f2-3b0b09a9bddd

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
1c055168-362e-469b-bc3b-997afe52b7f3
SPL ID
32f41ea8-ea6a-4526-b0f2-3b0b09a9bddd
Version
3
Effective date
2025-04-17
Source export date
2026-09-28
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/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:37:18

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 solution changes color or becomes cloudy • if you are sensitive or allergic to any ingredient in this product When using this product • to avoid contamination, do not touch tip of container to any surface • replace cap after each use Stop use and ask a doctor if • you experience eye pain • changes in vision occur • redness or irritation of the eye(s) gets worse or lasts more than 72 hours Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.