FDA label 4e10cc13-ee23-4d1d-a985-7b2b4c72a307

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
3eb3b2d8-3714-427e-8f69-3365940df750
SPL ID
4e10cc13-ee23-4d1d-a985-7b2b4c72a307
Version
7
Effective date
2015-01-06
Source export date
2026-09-28
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:39:38

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 muccous membranes Do not cover wit hbandage 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 doctor if conditions worsen, wymptoms persist for more tahn 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.