Lidocaine Menthol Pain Relief

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
Lidocaine Menthol Pain Relief
Generic name
LIDOCAINE, MENTHOL
Manufacturer
Amerisource Bergen
Product type
HUMAN OTC DRUG
SPL set ID
94039190-dde3-4d8e-873a-79abd3f6208b
SPL ID
52bfc22f-31a6-034f-e063-6394a90ab7d0
Version
6
Effective date
2026-05-26
Source export date
2026-10-27
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/2026-10-27/b7a5e61d87a3b8f87f4c3ff7b526bfbf6baf84c840f565574c7d83d4083e2b38/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run
20261027T193451Z
Imported at
2026-10-27 20:49:35
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS For External use only. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away. ■over raw surfaces or blistered areas If pregnant or breast feeding ask a health professional before use. WHEN USING: avoid contact with the eyes do not use more than one patch on your body at a time Stop use and consult a doctor if skin irritation develops condition worsens symptoms persist for more than 7 days or clear up and occur again within a few days

Reported adverse events (FAERS/openFDA)#

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