FDA label 59f97c3f-b22b-c425-e063-6394a90ae39b

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
7376b806-8e34-4c30-a902-1354edbde771
SPL ID
59f97c3f-b22b-c425-e063-6394a90ae39b
Version
8
Effective date
2026-08-26
Source export date
2026-10-27
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/2026-10-27/eeb012fd0992efa4f76b2aef09dd5f84150b96392c46717c44deabcc4e3581c1/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run
20261027T193451Z
Imported at
2026-10-27 20:39:43

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. Ask a doctor before use if you have narrow angle glaucoma When using this product: To avoid contamination, do not touch tip of container to any surface. Replace cap after using. Overuse of this product may produce increased redness of the eye. Pupils may become enlarged temporarily. Stop use & as k a doctor if: you experience eye pain you experience changes in vision you experience continued redness or irritation of the eye the condition worsens symptoms last for more than 72 hours Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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