FDA label 3d2291df-7967-45b0-875a-d0b01faf5648

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
be131aa0-5c1a-44dd-9420-be412765bf2c
SPL ID
3d2291df-7967-45b0-875a-d0b01faf5648
Version
2
Effective date
2022-01-24
Source export date
2026-11-06
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/824fe785252d7061429a95ddb6de517ee399ef628d34e8fdcc3591ded286ae33/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:23:15

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.