FDA.reportPublic FDA data

FDA label 689f6587-8f09-93f8-e053-2991aa0aa8ce

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
ea577bbb-81fa-499c-a3ae-12765bca4eb5
SPL ID
689f6587-8f09-93f8-e053-2991aa0aa8ce
Version
3
Effective date
2018-03-30
Source export date
2026-09-28
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:42:21

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. •Avoid contact with eyes. •Do not apply to wounds or damaged skin. •Do not use with bandage, wrap, brace, stocking or similar device or garment. •Do not use in combination with any other external analgesic products. •If symptoms persist for more than seven days, discontinue use and consult a physician. • Keep out of reach of children . If swallowed, consult physician. •Do not bandage tightly. •If pregnant of breast feeding, contact physician prior to use.

Reported adverse events (FAERS/openFDA)#

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