Home NDC 80425-0506 LidoPro Patch (Lidocaine 4%, Menthol 1%)
Product NDC 80425-0506
11-digit product format 804250506
Labeler code 80425
Product ID 80425-0506_30c9764f-80a6-7ffc-e063-6294a90a0c59
Type HUMAN OTC DRUG
Nonproprietary name Lidocaine and Menthol Patch
Dosage form PATCH
Route TRANSDERMAL
Labeler Advanced Rx of Tennessee, LLC
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-03-20
Substance MENTHOL; LIDOCAINE
Active strength 84; 336 mg/8400mg; mg/8400mg
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 LidoPro Patch (Lidocaine 4%, Menthol 1%)
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL 84 mg/8400mg LIDOCAINE 336 mg/8400mg
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination L7T10EIP3A Internal UNII lookup 98PI200987 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1249758 Internal RxNorm lookup 2675625 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 80425-0506-1 LidoPro Patch (Lidocaine 4%, Menthol 1%) 15 mg in 1 POUCH PATCH 15 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 80425-0506 LIDOPRO PATCH (LIDOCAINE 4%, MENTHOL 1%) (LIDOCAINE AND MENTHOL PATCH) PATCH [ADVANCED RX OF TENNESSEE, LLC] 1 Current NDC, 1 package rows 20250322_30c97646-db06-df84-e063-6394a90a7743.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 18 of 153 · 3,057 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 80425-0506-1 80425050601 15 mg in 1 POUCH (80425-0506-1) 15 mg 2025-03-20 No No Current