Lidonex

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
Lidonex
Generic name
LIDOCAINE HCL, MENTHOL
Manufacturer
Aldama Pharmaceuticals, Inc
Product type
HUMAN OTC DRUG
SPL set ID
365cf19c-70e0-c4e9-e063-6294a90ac428
SPL ID
587aebb8-055f-b485-e063-6394a90acf8c
Version
4
Effective date
2026-08-07
Source export date
2026-09-28
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:28:57
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 Flammable: Keep away from fire or flame Do not use on wounds or damaged skin in large quantaties with a heating pad if you are allergic to any ingredients of this product When using this product use only as directed. avoid contact with the eyes, mucous membranes or rashes do not bandage tightly Stop use and ask doctor if skin reactions occur, such as rash, itching, redness, irritation, pain, swelling and blistering condition worsens symptoms persist for more than 7 days symptoms 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.