FDA label cf626574-6a68-4fcd-9986-c036cbec8cf1

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
fea8eecc-594e-400b-9f1c-f888dbcd2b0b
SPL ID
cf626574-6a68-4fcd-9986-c036cbec8cf1
Version
1
Effective date
2015-07-22
Source export date
2026-11-06
Source partition
2
Source file
https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/4dafeb36642dffb72e2138939a956de402f722ea8c14c08cd87068efd3669f01/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 06:53:11

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 When Using this product • Use only as directed • Do not bandage tightly • Do not use with a heating pad • Avoid contact with eyes and mucous membranes • Do not apply to wounds, damaged, broken or irritated skin • A transient burning sensation may occur upon application but generally disappears in several days • If severe burning sensation occurs, discontinue use immediately and read package insert for important information • Do not expose the area treated with product to heat or direct sunlight • Avoid taking a bath or shower within 1 hour before or after applying

Reported adverse events (FAERS/openFDA)#

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