FDA label ae8c39a3-2e3c-4965-9bbe-725973ae9250

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
32aca040-37f7-4195-8a5f-332d589a64d8
SPL ID
ae8c39a3-2e3c-4965-9bbe-725973ae9250
Version
5
Effective date
2024-11-27
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 01:57:17

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 • on wounds or damaged skin • if you are allergic to Menthol When using this product • do not cover with bandage • use only as directed • avoid contact with eyes and mucous membranes 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 • rash, itching or excessive skin irritation occurs

Reported adverse events (FAERS/openFDA)#

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