LidoPlus 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: LidoPlus Pain Relief
Generic name: LIDOCAINE HYDROCHLORIDE
Manufacturer: Centura Pharmaceuticals, Inc
Product type: HUMAN OTC DRUG
SPL set ID: 07bacc6c-60a6-4297-8663-904a22bdc040
SPL ID: 48355fe4-49c2-3ad4-e063-6294a90a215f
Version: 7
Effective date: 2026-01-12
Source export date: 2026-10-27
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/d7629e6f844435cfe6cb0cf8c5341c46775ea16c5af42c77a22a2ffe820a2cd2/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 19:52:44

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 · 13 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		LidoPlus Pain Relief	openfda.brand_name
generic name		LIDOCAINE HYDROCHLORIDE	openfda.generic_name
manufacturer name		Centura Pharmaceuticals, Inc	openfda.manufacturer_name
ndc	package	70372-723-02	openfda.package_ndc
ndc	package	70372-723-01	openfda.package_ndc
ndc	product	70372-723	openfda.product_ndc
ndc11	package	70372072301	derived:openfda.package_ndc
ndc11	package	70372072302	derived:openfda.package_ndc
rxcui		1010895	openfda.rxcui
spl id		48355fe4-49c2-3ad4-e063-6294a90a215f	id
spl set id		07bacc6c-60a6-4297-8663-904a22bdc040	set_id
unii		V13007Z41A	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. • Avoid contact with eyes. • If condition worsens or symptoms persist for more than seven days, discontinue use and consult physician. Keep out of reach of children. If swallowed, consult physician. Do not use in large quantities, particularly over raw surfaces or blistered areas. If pregnant or breast feeding, contact physician prior to use.

Reported adverse events (FAERS/openFDA)#

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