FDA.reportPublic FDA data

LM Plus Relief

Product NDC
71436-3571
Requested package NDC
71436-3571-5
11-digit product format
714363571
Labeler code
71436
Product ID
71436-3571_27fac912-0cb1-4cbd-b500-ce1a224cd965
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Lidocaine and Menthol
Dosage form
PATCH
Route
TOPICAL
Labeler
ARI BRANDS, LLC
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2023-09-01
Substance
LIDOCAINE; MENTHOL
Active strength
490; 980 mg/1; mg/1
Pharmacologic classes
Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product
Yes
Brand name base
LM Plus Relief
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
LIDOCAINE490 mg/1
MENTHOL980 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
98PI200987Internal UNII lookup
L7T10EIP3AInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
2199672Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
e9b52074-b4ca-43e9-9f2e-2afcdb5efdc7Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71436-3571-5LM Plus Relief5 in 1 POUCHPATCH51
71436-3571-5LM Plus Relief3 in 1 CARTONPATCH31

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
71436-3571-5EA - Each71436-3571da11c400-a463-4563-b166-917344a7a93512023-12-05

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71436-3571LM PLUS RELIEF (LIDOCAINE AND MENTHOL) PATCH [ARI BRANDS, LLC]1Current NDC, 2 package rows20231025_e9b52074-b4ca-43e9-9f2e-2afcdb5efdc7.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
LM Plus ReliefLIDOCAINE AND MENTHOLARI BRANDS, LLCe9b52074-b4ca-43e9-9f2e-2afcdb5efdc72023-09-01Warnings, Adverse reactionsExact identifier
ndc (package): 71436-3571-5
ndc (product): 71436-3571
ndc11 (package): 71436357105

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
2199672lidocaine 3.5 % / menthol 7 % Medicated PatchPSNe9b52074-b4ca-43e9-9f2e-2afcdb5efdc71
2199672lidocaine 0.035 MG/MG / menthol 0.07 MG/MG Medicated PatchSCDe9b52074-b4ca-43e9-9f2e-2afcdb5efdc71
2199672lidocaine 3.5 % / menthol 7 % Medicated PatchSYe9b52074-b4ca-43e9-9f2e-2afcdb5efdc71

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
71436-3571-5714363571053 POUCH in 1 CARTON (71436-3571-5) / 5 PATCH in 1 POUCH3 pouch2023-09-01NoNoCurrent