Home NDC 70372-723 LidoPlus Pain Relief
Product NDC 70372-723
11-digit product format 703720723
Labeler code 70372
Product ID 70372-723_48355fe4-49c2-3ad4-e063-6294a90a215f
Type HUMAN OTC DRUG
Nonproprietary name LIDOCAINE HYDROCHLORIDE
Dosage form CREAM
Route TOPICAL
Labeler Centura Pharmaceuticals, Inc
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2015-12-25
Substance LIDOCAINE HYDROCHLORIDE
Active strength 40 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 LidoPlus Pain Relief
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength LIDOCAINE HYDROCHLORIDE 40 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 RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1010895 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 70372-723-01 LidoPlus Pain Relief 118 mL in 1 TUBE CREAM 118 7 70372-723-01 LidoPlus Pain Relief 1 in 1 BOX CREAM 1 7 70372-723-02 LidoPlus Pain Relief 5 mL in 1 PACKET CREAM 5 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70372-723 LIDOPLUS PAIN RELIEF (LIDOCAINE HYDROCHLORIDE) CREAM [CENTURA PHARMACEUTICALS, INC] 6 Current NDC, Legacy NDC, 3 package rows 20250129_07bacc6c-60a6-4297-8663-904a22bdc040.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 Marketing end Sample Exclude flag Status 70372-723-01 70372072301 1 TUBE in 1 BOX (70372-723-01) / 118 mL in 1 TUBE 1 tube 2017-02-07 0000-00-00 No No Current 70372-723-02 70372072302 5 mL in 1 PACKET (70372-723-02) 5 ml 2024-03-03 No No Current