FDA label 968aa925-85b3-7516-e053-2995a90a64e2

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
2a3f0a3e-3ae2-4d7e-e054-00144ff88e88
SPL ID
968aa925-85b3-7516-e053-2995a90a64e2
Version
4
Effective date
2019-11-04
Source export date
2026-09-28
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:09:48

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. In case of contact with eye in undiluted form, flush with clean water Do not use in full strength When using this product do not change dilution or use with other chemicals do not reuse Stop use and ask a doctor if you have any of the following changes in vision eye pain condition worsens or persists continued redness or irritations of the eye

Reported adverse events (FAERS/openFDA)#

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