FDA label 65613ee8-b892-42be-b345-8d55d36035dd

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
de464a61-5143-47de-b7c0-6d899cc535b6
SPL ID
65613ee8-b892-42be-b345-8d55d36035dd
Version
1
Effective date
2020-02-10
Source export date
2026-09-28
Source partition
1
Source file
https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/9c7783846d422acb0c9e59457606951c785a7d28cc631c8cc4839d0dc7c55f39/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:13:46

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: Flammable: Keep away from excessive heat or open flame. Ask a doctor before use if you have sensitive skin or if you are taking any blood thinners. When using this product Do not use on wounds or irritated skin Do not bandage tightly or use with a heating pad Wash hands after use with cool water If pregnant or breast feeding , ask a health professional before use Keep out of reach of children. If accidentally swallowed, contact a doctor or poison control center immediately Stop use and ask a doctor if condition worsens or if pain persists for more than 7 days, or clears up, then reoccurs within a few days.

Reported adverse events (FAERS/openFDA)#

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