FDA label 63e0e91e-6bbd-4d01-897e-052fa54da652

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
b6a85941-fb0f-4714-b2c8-a9482b2ffe04
SPL ID
63e0e91e-6bbd-4d01-897e-052fa54da652
Version
4
Effective date
2016-10-29
Source export date
2026-09-28
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/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:29:55

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 -Do not apply to open wounds or damages skin - If symptoms persist for more than seven days, discontinue use and consult a physician - Keep out of reach of children. If swallowed, consult physician - Do not bandage tightly - If pregnant or breast feeding, contact physician prior to use

Reported adverse events (FAERS/openFDA)#

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