Home NDC 87843-211 Lidocaine Patch 4%
Product NDC 87843-211
11-digit product format 878430211
Labeler code 87843
Product ID 87843-211_14e5eae6-bd6f-47b5-b8a3-10c2193f30c3
Type HUMAN OTC DRUG
Nonproprietary name Lidocaine 4%
Dosage form PATCH
Route TRANSDERMAL
Labeler Global America Group LLC
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-08-31
Substance LIDOCAINE
Active strength 40 mg/g
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 Patch 4%
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength LIDOCAINE 40 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 98PI200987 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1737778 Internal RxNorm 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 109 of 151 · 3,020 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 87843-211-30 87843021130 6 POUCH in 1 BOX (87843-211-30) / 5 g in 1 POUCH 6 pouch 2026-08-31 No No Current