FDA label 63eea2b9-bea1-4347-a6ed-222d5f749d86

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
5b171000-a3d7-4adf-817f-1eba14773e0a
SPL ID
63eea2b9-bea1-4347-a6ed-222d5f749d86
Version
4
Effective date
2017-12-20
Source export date
2026-10-12
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:34:18

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. • •Consult physician for children under 12. • •Do not use if you are allergic to 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 • •Or rash, itching or excessive skin irritation occurs.

Reported adverse events (FAERS/openFDA)#

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