LMX4

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: LMX4
Generic name: LIDOCAINE
Manufacturer: Ferndale Laboratories, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: f0e7c92f-8b0b-4045-b659-af9f6e81260f
SPL ID: 459c9507-ea18-81b1-e063-6394a90a3db4
Version: 6
Effective date: 2025-12-10
Source export date: 2026-09-28
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:54:48

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 22 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		LMX4	openfda.brand_name
generic name		LIDOCAINE	openfda.generic_name
manufacturer name		Ferndale Laboratories, Inc.	openfda.manufacturer_name
ndc	package	0496-0882-06	openfda.package_ndc
ndc	package	0496-0882-71	openfda.package_ndc
ndc	package	0496-0882-05	openfda.package_ndc
ndc	package	0496-0882-07	openfda.package_ndc
ndc	package	0496-0882-30	openfda.package_ndc
ndc	package	0496-0882-15	openfda.package_ndc
ndc	product	0496-0882	openfda.product_ndc
ndc11	package	00496088205	derived:openfda.package_ndc
ndc11	package	00496088207	derived:openfda.package_ndc
ndc11	package	00496088206	derived:openfda.package_ndc
ndc11	package	00496088215	derived:openfda.package_ndc
ndc11	package	00496088271	derived:openfda.package_ndc
ndc11	package	00496088230	derived:openfda.package_ndc
rxcui		1422103	openfda.rxcui
rxcui		1421893	openfda.rxcui
spl id		459c9507-ea18-81b1-e063-6394a90a3db4	id
spl set id		f0e7c92f-8b0b-4045-b659-af9f6e81260f	set_id
unii		98PI200987	openfda.unii

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 in or near the eyes in large quantities, particularly over raw surfaces or blistered areas Stop use and ask a doctor if: allergic reaction occurs condition worsens or does not improve within 7 days symptoms clear up and return within a few days redness, irritation, swelling, pain or other symptoms begin or increase

Reported adverse events (FAERS/openFDA)#

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