FDA label d417edfb-86ce-4554-b1ce-ce126af62abb

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
be26909d-afbb-4b89-a64a-fd130de223c7
SPL ID
d417edfb-86ce-4554-b1ce-ce126af62abb
Version
1
Effective date
2017-08-15
Source export date
2026-09-28
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:52:40

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: Use only as directed Do not use with a heating pad, may blister skin on open wounds or damaged skin Ask a doctor before use if you have redness over the affected area When using this product avoid contact with eyes do not bandage tightly Stop use and consult a doctor if skin redness or excessive skin irritation develops condition worsens or symptoms persist for more than 7 days symptoms clear up and occur again in a few days Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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