FDA label 23004824-ff50-63bc-e063-6394a90ae46f

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
23004824-ff4f-63bc-e063-6394a90ae46f
SPL ID
23004824-ff50-63bc-e063-6394a90ae46f
Version
1
Effective date
2024-09-26
Source export date
2026-10-12
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:56:39

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

Warning 1. For external use only, use withcaution when the skin haswounds, swelling, or pus;2. This product may cause allergicreactions to a small number ofpeople, please stop using itimmediately if you feel unwell.Before each use, please select asmall piece of skin for an allergytest. There is no adverse skinreaction 24 hours before usingthis product;3.Use according to theinstructions.

Reported adverse events (FAERS/openFDA)#

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