Mentholatum Lidocaine Ice

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)

Brand name
Mentholatum Lidocaine Ice
Generic name
LIDOCAINE HCL, MENTHOL
Manufacturer
The Mentholatum Company
Product type
HUMAN OTC DRUG
SPL set ID
4d74cbab-31cd-4579-9360-6852ee215b5e
SPL ID
292c447d-ea07-2df7-e063-6294a90aabf6
Version
5
Effective date
2024-12-13
Source export date
2026-09-28
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:15:49
Harmonized routes table
Harmonized routes
TOPICAL

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 large areas of the body or on cut, irritated or blistered skin on puncture wounds for more than one week without consulting a doctor When using this product use only as directed do not get into eyes do not bandage tightly or apply external heat to the area of use Stop use and ask a doctor if condition worsens symptoms persist for more than 7 days or clear up and occur again within a few days redness, rash, or irritation occurs

Reported adverse events (FAERS/openFDA)#

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