FDA.reportPublic FDA data

FDA label 28ed0c14-f439-7e8f-e063-6294a90aafa8

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
e7836f22-4017-415f-b8f0-54b07b6d6c00
SPL ID
28ed0c14-f439-7e8f-e063-6294a90aafa8
Version
16
Effective date
2024-12-10
Source export date
2026-10-12
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/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:55:53

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. avoid contact with eyes and mucous membranes. do not cover with bandage. do not use on wounds or damaged skin. keep out of reach of children. consult physician for children under 12. do not use if you are allergic to methyl salicylate or menthol. stop use and ask a doctor if conditions worsen, symptoms persist for more than 7 days or clear up and occur again within a few days. if rash, itching or excessive skin irritations occurs.

Reported adverse events (FAERS/openFDA)#

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