FDA label dd23b911-42c0-4544-af0d-a837bd711fc9

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
945c211a-324a-40e1-ba83-3fd0cba4ebd4
SPL ID
dd23b911-42c0-4544-af0d-a837bd711fc9
Version
3
Effective date
2014-08-04
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 01:49:48

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 Avoid contact with eyes Stop use and ask a doctor if condition worsens, symptoms last more than 7 dasy or clear up and occure again within a few days Do not use on deep puncture wounds, animal bites, serious burns If pregnant or breast feeding, contact physician prior to use Do not use in large quantities, particularly over raw sufaces or blistered areas

Reported adverse events (FAERS/openFDA)#

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