FDA label c04c298d-b275-4a45-8bc3-4f53dff5b5a1

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
ecc8f4c5-2ccb-4d54-a3c1-b9b8d0ad8a50
SPL ID
c04c298d-b275-4a45-8bc3-4f53dff5b5a1
Version
1
Effective date
2019-04-08
Source export date
2026-10-12
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b939c18fdf51df171cf60ce5558819d08ac66bb16bb9991d48cbec91028d783e/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:36:50

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 is 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 usewith 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.