Dermatool Nerve Care

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
Dermatool Nerve Care
Generic name
LIDOCAINE HCL, MENTHOL
Manufacturer
Papalo Group, LLC
Product type
HUMAN OTC DRUG
SPL set ID
4ee40c96-9350-4c68-e063-6294a90ac812
SPL ID
4ee40c96-9351-4c68-e063-6294a90ac812
Version
1
Effective date
2026-04-07
Source export date
2026-09-28
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:26:28
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

For external use only. Do not use if you have had an allergic reaction to lidocaine or other local anesthetics, on large areas of the body or on cut, irritated, blistered, or swollen skin, on puncture wounds, for more than one week without consulting a doctor. When using this product only use as directed. Read and follow all directions and warnings on this carton, avoid contact with eyes and mucous membranes, rar cases of serious burns have been reported with products of this type, do not apply to wounds or damaged, broken or irritated skin, do not bandage tightly or apply local heat (such as heating oads) or a medicated patch to the area of use, a transient burning sensation may occur upon application but generally disappears in serval days, avoid applyin ginto skin folds. Stop use and ask a doctor if the condition worsens, symptoms persist for more than 7 days or clear up and occur again within a few days, you experience signs of skin injury, such as pain, swelling, or blistering where the product was applied.

Reported adverse events (FAERS/openFDA)#

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