FDA label 6040b4ad-a872-004e-e053-2a91aa0ae787

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
cd8cb7a8-084d-4a1b-9302-911f7a6330c8
SPL ID
6040b4ad-a872-004e-e053-2a91aa0ae787
Version
6
Effective date
2017-12-13
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 06:12:01

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

External use only 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: temporoary burning and iritation upon being instilled into eye may occur To avoid contamination, do not touch top of container to any surface Replace cap after using, keep tightly closed In case of accidental ingestion, seek professional help or contact a Poision Control Center immediately. Stop use and ask a doctor if: you experience eye pain, changes in vision, continued redness, or irritation of the eye. if the condition worses or persists

Reported adverse events (FAERS/openFDA)#

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