FDA label d351e6e5-1091-47bf-8f06-cee53dc84e63

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
85933294-59de-4465-a02c-4225f0c20ce8
SPL ID
d351e6e5-1091-47bf-8f06-cee53dc84e63
Version
2
Effective date
2015-03-24
Source export date
2026-09-28
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:51:42

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.