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
2026-11-06
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/2026-11-06/824fe785252d7061429a95ddb6de517ee399ef628d34e8fdcc3591ded286ae33/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:25:23

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.