FDA label f03f6245-da64-42ce-bc38-8cc774990b6a

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
4d5c8d59-a968-4d96-a4a0-04b34ed08596
SPL ID
f03f6245-da64-42ce-bc38-8cc774990b6a
Version
1
Effective date
2016-09-15
Source export date
2026-11-06
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/2026-11-06/97001096994db9ca8cee114e6c3bb5298d3c573158ffc1ab8692d82e76a3eb40/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 06:57:23

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. do not apply to wounds or damaged skin do not bandage tightly do not use with heating pad, pack, wrap, hot water bottle or any heating element When using this product do not get into eyes avoid contact with other mucous membranes Discontinue use and ask a doctor if condition worsens or if symptoms persist for more than 7 days or clear up and occur again within a few days Keep out of reach of children. if swallowed, get medical help or contact a Poison Control center right away if pregnant or nursing, seek the advice of a health professional before using

Reported adverse events (FAERS/openFDA)#

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