FDA label 9038d6cb-1626-442f-aaf5-2cc07072639d

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
0dd90118-0013-9bf2-e063-6394a90afe3c
SPL ID
9038d6cb-1626-442f-aaf5-2cc07072639d
Version
2
Effective date
2024-12-12
Source export date
2026-10-12
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/2026-10-12/7928c8e8c6256620071a8b7e5b93eb8dfa543649c08d17a01ea02251012ba58c/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:25:18

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 use in eyes only. • Using this product , to avoid contamination, do not touch tip of container to any surface. • Do not reuse. Once opened, discard after use. • Do not touch single-use container tip to the eye. Stop use and ask a doctor if • You experience eye pain, changes in vision, continued redness, or irritation of the eye. • The condition worsens or persists for more than 72 hours. Keep out of reach of children. Keep this and all drugs out of the reach of children . If swallowed, get medical help or contact a Poison Control Center immediately (1-800-222-1222).

Reported adverse events (FAERS/openFDA)#

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