FDA label ce7d5be7-57b3-41d3-a591-5483cab4fbf9

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
c52d4d06-b8df-479c-ab4b-dce88ae49c9d
SPL ID
ce7d5be7-57b3-41d3-a591-5483cab4fbf9
Version
3
Effective date
2011-08-26
Source export date
2026-10-12
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:08:09

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 Do not use with other topical pain relievers, with heating pads or heating devices When using this product do not use in or near eyes, do not apply to wounds or damaged skin do not bandage tightly Stop use and ask doctor if condition worsens, symptoms last more than days or clear up and occur again within a few days, redness or irritation develops If pregnant or breast feeding ask a health professional before use.

Reported adverse events (FAERS/openFDA)#

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