FDA.reportPublic FDA data

FDA label 2c499ed7-e4d6-48b4-a6b7-4ac80fef02d7

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
e5d8418c-d928-4fd1-84f0-78a1e772ee5c
SPL ID
2c499ed7-e4d6-48b4-a6b7-4ac80fef02d7
Version
5
Effective date
2016-09-07
Source export date
2026-09-28
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/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:21:57

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 mucus 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 Menthol. Stop use ad ask a doctor if condition worsens, symptoms persist for more than 7 days or clear up and occur again within a few days. or a rash, itching or excessive skin irritation occurs.

Reported adverse events (FAERS/openFDA)#

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