Home NDC 83602-211 Lidocaine Plantar Relief Roll-On
Product NDC 83602-211
11-digit product format 836020211
Labeler code 83602
Product ID 83602-211_585ccb4b-3c00-39b9-e063-6294a90a0e18
Type HUMAN OTC DRUG
Nonproprietary name Lidocaine
Dosage form GEL
Route TOPICAL
Labeler Guangzhou Liuquanmiao Import & Export Trade Co., Ltd.
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-08-06
Substance LIDOCAINE HYDROCHLORIDE
Active strength 39.2 mg/mL
Pharmacologic classes Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]
NDC exclude flag No
Listing certified through 2027-12-31
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 Lidocaine Plantar Relief Roll-On
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength LIDOCAINE HYDROCHLORIDE 39.2 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination V13007Z41A Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 8 of 156 · 3,115 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 83602-211-73 83602021173 1 BOTTLE in 1 BOX (83602-211-73) / 73 mL in 1 BOTTLE 1 bottle 2026-08-06 No No Current