FDA label 293511a9-f404-3632-e063-6394a90a79f0

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
3801584a-6212-4ad0-8d6e-ef60e7edae14
SPL ID
293511a9-f404-3632-e063-6394a90a79f0
Version
6
Effective date
2024-12-14
Source export date
2026-10-12
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:31:15

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 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 use if you have a known allergy to any of the ingredients listed. - 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.