FDA label f9babc71-ef7f-478f-b327-c4aee64ff8c8

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
2dfeea72-4e24-443c-95e9-b5073b486e86
SPL ID
f9babc71-ef7f-478f-b327-c4aee64ff8c8
Version
2
Effective date
2022-01-25
Source export date
2026-10-30
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-30/a3e33fe073aa0aa94eb690c6684c74434c63cebfbf7c5530205a2c3e957ecb8b/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run
20261102T182004Z
Imported at
2026-11-02 19:47:31

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.