Home NDC 80425-0452 LidoPro Pain Relief
Product NDC 80425-0452
11-digit product format 804250452
Labeler code 80425
Product ID 80425-0452_2bc81112-204c-2514-e063-6394a90a80ed
Type HUMAN OTC DRUG
Nonproprietary name Capsaicin and Lidocaine
Dosage form OINTMENT
Route TRANSDERMAL
Labeler Advanced Rx of Tennessee, LLC
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-11-26
Substance MENTHOL, (+)-; LIDOCAINE HYDROCHLORIDE; METHYL SALICYLATE; CAPSAICIN
Active strength 10; 4; 27.5; .0325 mg/100mg; mg/100mg; mg/100mg; mg/100mg
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 Pain Relief
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL, (+)- 10 mg/100mg LIDOCAINE HYDROCHLORIDE 4 mg/100mg METHYL SALICYLATE 27.5 mg/100mg CAPSAICIN .0325 mg/100mg
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 matching rows.
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 80425-0452-1 LidoPro Pain Relief 9900 mg in 1 TUBE, WITH APPLICATOR OINTMENT 9900 2 80425-0452-1 LidoPro Pain Relief 1 in 1 BOX OINTMENT 1 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 80425-0452 LIDOPRO PAIN RELIEF (CAPSAICIN AND LIDOCAINE) OINTMENT [ADVANCED RX OF TENNESSEE, LLC] 2 Current NDC, 2 package rows 20250117_27d5997b-1cc2-41c2-e063-6394a90ac74a.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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Sample Exclude flag Status 80425-0452-1 80425045201 1 TUBE, WITH APPLICATOR in 1 BOX (80425-0452-1) / 9900 mg in 1 TUBE, WITH APPLICATOR 2024-11-26 No No Current