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
2026-09-28
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 06:17:48
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. 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.