FDA.reportPublic FDA data

FDA label d0268ec9-6850-4c69-b80d-f7b2017725fc

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
c4cd6323-320b-4a0b-af78-63be4cda23ba
SPL ID
d0268ec9-6850-4c69-b80d-f7b2017725fc
Version
3
Effective date
2017-11-08
Source export date
2026-10-12
Source partition
13
Source file
https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b8dac220ac9fc8ffb4d86c6e00ece30169fc4575ca0cc92e5c9ce1a524fb0249/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 03:02:11

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 • use only as directed • do not use at least 1 hour before, or immediately after, a bath or shower • do not get into eyes or on mucous membranes • do not apply to wounds or to damaged or very sensitive skin • do not bandage tightly or cover with any type of wrap except clothing • do not use with a heating pad or apply external heat • do not use in combination with other external analgesic products Stop use and ask a doctor if • condition worsens • excessive irritation, burning or discomfort of the skin develops • pain persists for more than 7 days • symptoms clear up and occur again within a few days

Reported adverse events (FAERS/openFDA)#

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