FDA label 23a7cdb9-69ea-378d-e063-6394a90a0f01

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
29ebc5dd-9d57-43b4-a7ce-4ea6d8b280cb
SPL ID
23a7cdb9-69ea-378d-e063-6394a90a0f01
Version
3
Effective date
2024-10-04
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 01:32:07

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 or mucous membranes Do not apply to open wounds or damaged skin Do not bandage or use heating pad Do not use on large areas of the body or on cut, irritated or swollen skin on puncture wounds for more than one week without consulting a doctor Stop use and ask a doctor if Condition worsens servere skin irritation occurs Symptoms persist for more than 7 days or clear up then reoccur again within a few days Ask a doctor before use if you Have sensitive skin Are pregnant or breastfeeding

Reported adverse events (FAERS/openFDA)#

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