FDA label 514301b8-470b-47ff-b6ab-8c20e85f36ac

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
6e4a94d3-ae02-406a-bee1-0d9d85ab6b93
SPL ID
514301b8-470b-47ff-b6ab-8c20e85f36ac
Version
6
Effective date
2014-03-31
Source export date
2026-10-12
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:50:15

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 2 matching rows.

warnings

Warnings For external use only. Avoid contact with eyes. In case of eye contact, rinse thoroughly with water. Discontinue use if irritation and redness develops. Consult a doctor if condition persists for more than 72 hours. If swallowed, immediately call Poison Control Center or doctor.

warnings

Warnings For external use only. Avoid contact with eyes. In case of eye contact, rinse thoroughly with water. Discontinue use if irritation and redness develops. Consult a doctor if condition persists for more than 72 hours. If swallowed, immediately call Poison Control Center or doctor.

Reported adverse events (FAERS/openFDA)#

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