Home NDC 72188-170 MAXOCAINE PAIN RELIEVING ROLL-ON
Product NDC 72188-170
11-digit product format 721880170
Labeler code 72188
Product ID 72188-170_09dc681e-2348-4213-e063-6394a90a41e1
Type HUMAN OTC DRUG
Nonproprietary name LIDOCAINE HYDROCHLORIDE, MENTHOL
Dosage form LIQUID
Route TOPICAL
Labeler Prime Commerce, LLC
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2018-03-01
Substance LIDOCAINE HYDROCHLORIDE; MENTHOL
Active strength 40; 10 mg/mL; mg/mL
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 MAXOCAINE PAIN RELIEVING ROLL-ON
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength LIDOCAINE HYDROCHLORIDE 40 mg/mL MENTHOL 10 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination V13007Z41A Internal UNII lookup L7T10EIP3A Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2002008 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 72188-170-03 MAXOCAINE PAIN RELIEVING ROLL-ON 88 mL in 1 BOTTLE, WITH APPLICATOR LIQUID 88 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72188-170 MAXOCAINE PAIN RELIEVING ROLL-ON (LIDOCAINE HYDROCHLORIDE, MENTHOL) LIQUID [PRIME COMMERCE, LLC] 3 Current NDC, Legacy NDC, 1 package rows 20231112_c263d5f2-89b9-4dfd-91c8-f894e5f956c9.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 48 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 72188-170-03 72188017003 88 mL in 1 BOTTLE, WITH APPLICATOR (72188-170-03) 88 ml 2018-03-01 0000-00-00 No No Current