FDA label ab0d2fbf-ceda-4085-b84b-4f436d2e4ae5

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
0382e535-3d6c-40fc-bf85-632f0b675c30
SPL ID
ab0d2fbf-ceda-4085-b84b-4f436d2e4ae5
Version
2
Effective date
2022-01-25
Source export date
2026-09-28
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:31:46

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 breastfeeding: 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.