FDA label 8032ce8e-52a8-4909-b8e4-cabfb5f75a35

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
57057b75-bad3-4089-980a-669b2ab6c33a
SPL ID
8032ce8e-52a8-4909-b8e4-cabfb5f75a35
Version
6
Effective date
2013-07-19
Source export date
2026-10-12
Source partition
13
Source file
https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b8dac220ac9fc8ffb4d86c6e00ece30169fc4575ca0cc92e5c9ce1a524fb0249/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 03:04:05

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. Use only if single-use dropper is intact. To avoid contamination, do not touch the tip of the dropper to any surface. Do not reuse. Once opened, discard. Contact wearers: consult a physician prior to using. Do not use: if the solution changes color or becomes cloudy Stop use and ask a doctor if: symptoms worsen or persist for more than 72 hours. changes in vision occur. you experience eye pain. If pregnant or breast feeding, ask a health professional before use. 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.