FDA.reportPublic FDA data

FDA label f90d372b-be90-4f62-b6ba-49f0e2e4efa5

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
8459a675-dc5c-4fe1-a54c-37ad0db43a49
SPL ID
f90d372b-be90-4f62-b6ba-49f0e2e4efa5
Version
1
Effective date
2015-01-09
Source export date
2026-09-28
Source partition
9
Source file
https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:59:42

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. • KEEP OUT OF REACH OF CHILDREN

Reported adverse events (FAERS/openFDA)#

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