FDA label 293511a9-f407-3632-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
0096cca7-5671-4717-bc92-12170c1bcf2f
SPL ID
293511a9-f407-3632-e063-6394a90a79f0
Version
5
Effective date
2024-12-14
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 01:55:48

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

For external use only When using this product Read inside of carton before using Use only as directed Do not bandage tightly or cover treated areas Do not use with heating pad Avoid contact with eyes and mucous membranes Do not apply to wounds or damaged, broken or irritated skin A mild burning sensation may occur. If severe burning sensation occurs, discontinue use immediately If symptoms persist for more than seven days, discontinue and consult physician Keep out of reach of children If swallowed, consult physician 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.