FDA.reportPublic FDA data

FDA label 1eece9ed-dcf6-0c2b-e054-00144ff88e88

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
4620bf58-6b97-4927-bb0e-dde71f38da83
SPL ID
1eece9ed-dcf6-0c2b-e054-00144ff88e88
Version
3
Effective date
2015-09-04
Source export date
2026-09-28
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:11:18

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 Do not apply to open wounds or damaged skin. If symptoms persist for more than seven days, discontinue use and consult 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. Do not use in large quantities, particularly over raw surfaces or blistered areas.

warnings and cautions

Do not bandage tightly If pregnant or breast feeding, contact physician prior to use. Do not use in large quantities, particularly over raw surfaces or blistered areas.

Reported adverse events (FAERS/openFDA)#

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