FDA.reportPublic FDA data

FDA label 0dcb705d-cf61-45a8-937d-96ce6b873cfa

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
1ef21407-5fd2-4349-8d4f-af3b13dab476
SPL ID
0dcb705d-cf61-45a8-937d-96ce6b873cfa
Version
5
Effective date
2024-11-27
Source export date
2026-11-06
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/2026-11-06/10387d7618367cd955339e75d48af3d11f99f789153db05c529d9fad6eccc645/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:15:59

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 Do not use • if pregnant or breastfeeding, consult physician prior to use • in large quantities, particularly over raw surfaces or blistered areas When using this product • use only as directed • do not bandage tightly • avoid contact with eyes • do not apply to open wounds or damaged skin Stop use and ask a doctor if • symptoms persist for more than seven days, discontinue use and consult physician • swallowed, consult physician

Reported adverse events (FAERS/openFDA)#

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