FDA.reportPublic FDA data

FDA label 65986bc2-c2e7-345e-e053-2991aa0ad094

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
5a5a8ce6-2c7b-e078-e053-2991aa0a0e3a
SPL ID
65986bc2-c2e7-345e-e053-2991aa0ad094
Version
2
Effective date
2018-02-19
Source export date
2026-08-17
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/2026-08-17/1b5caad1d26c65d5be0ee71b8eb1373f0c7d99e6d83d2bfe99382f282ec02e02/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
ca19d5b1416b6b66a9d383bfdc77d90e91adfeefe16ffcc1ac6b06ceb90d8d73
Import run
20260818T065550Z
Imported at
2026-08-18 07:45:03

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

Warning : for external use only Use only as directed. Avoid contact with the eyes and mucous membranes. DO not apply to open wounds, damaged or very sensitive skin. Test on a small area before use. Do not use in combination with other external analgesic products. Do not bandage tightly or cover with any type of wrap, except clothing. If condition worsens, or persists for more than seven days, discontinue use and consult a physician.