FDA label 01a8dedc-8c60-4060-a49b-70f8d53db07d

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
ab12c419-4b1a-4119-9e23-76ce7a89d1a7
SPL ID
01a8dedc-8c60-4060-a49b-70f8d53db07d
Version
8
Effective date
2022-07-01
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 05:17:38

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 Do not use this product except under the advice and supervision of a doctor. if imprinted seal is broken or missing. if solution changes color or becomes cloudy. When using this product temporary burning and irritation upon being instilled into eye may occur. 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. you experience changes in vision. redness or irritation of the eye continues condition worsens or persists. 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.