FDA label 8f3d7a8b-2852-46af-9c97-5bb23b1c4f8b

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
88cae062-ea96-4de1-9930-dbfc406a6180
SPL ID
8f3d7a8b-2852-46af-9c97-5bb23b1c4f8b
Version
2
Effective date
2013-07-11
Source export date
2026-10-12
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/13cbfcd236c665f0ee69e2d9141331148dcdff45d1679c92f029cfba27dd74a2/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:41:41

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. Initial exacerbation of symptoms may occur. Replace cap tightly after every use. To avoid contamination, do not touch the tip of the container to any surface. Use within 30 days of opening. Expiration date only refers to unopened bottle. Contact wearers: consult a physician prior to using. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. Do not use: if the solution changes color or becomes cloudy Stop use and ask a doctor if: changes in vision occur the child experiences eye pain the child experiences continued redness or irritation of the eye symptoms worsen or persist for more than 72 hours

Reported adverse events (FAERS/openFDA)#

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