Home NDC 51142-652-28 Antibacterial Lidocaine Wound Gel
Product NDC 51142-652
Requested package NDC 51142-652-28
11-digit product format 511420652
Labeler code 51142
Product ID 51142-652_262f971a-aa6f-8cd4-e063-6394a90a40b0
Type HUMAN OTC DRUG
Nonproprietary name benzalkonium chloride, lidocaine hydrochloride
Dosage form GEL
Route TOPICAL
Labeler ASO LLC
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-10-28
Substance LIDOCAINE HYDROCHLORIDE; BENZALKONIUM CHLORIDE
Active strength 2; .13 g/100mL; g/100mL
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 Antibacterial Lidocaine Wound Gel
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength LIDOCAINE HYDROCHLORIDE 2 g/100mL BENZALKONIUM CHLORIDE .13 g/100mL
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 F5UM2KM3W7 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1431682 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 51142-652-14 Antibacterial Lidocaine Wound Gel 1 in 1 CARTON GEL 1 3 51142-652-14 Antibacterial Lidocaine Wound Gel 14 mL in 1 TUBE GEL 14 3 51142-652-28 Antibacterial Lidocaine Wound Gel 1 in 1 CARTON GEL 1 3 51142-652-28 Antibacterial Lidocaine Wound Gel 28 mL in 1 TUBE GEL 28 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 51142-652 ANTIBACTERIAL LIDOCAINE WOUND GEL (BENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE) GEL [ASO LLC] 3 Current NDC, Legacy NDC, 4 package rows 20241107_cb9505b7-222d-3a24-e053-2a95a90a0b64.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 119 of 151 · 3,010 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Meijer Cold and Hot Pain Relieving Analgesic LIDOCAINE HYDROCHLORIDE AND MENTHOL, UNSPECIFIED FORM Meijer Distribution, Inc 6d356563-9098-4994-8ad8-819a8033a9f4 2024-11-06 Warnings Exact identifier application number: M017 TopCare Maximum Strength Pain Relieving Analgesic MENTHOL, UNSPECIFIED FORM Topco Associates LLC dc80d2f9-e3eb-4feb-bad5-7d6ab107f9ab 2024-11-05 Warnings Exact identifier application number: M017 Aveeno Restorative Skin Therapy Itch Relief Balm PRAMOXINE HYDROCHLORIDE Kenvue Brands LLC 61824ca7-a2d3-4830-b2bb-149a3222bfc8 2024-11-05 Warnings Exact identifier application number: M017 Aveeno Hydrocortisone ANTI-ITCH HYDROCORTISONE Kenvue Brands LLC 233de4d7-e533-40cd-a5ed-e8b09abc626e 2024-11-05 Warnings Exact identifier application number: M017 STING MASTER LIDOCAINE HYDROCHLORIDE Les Technologies Ptero, Inc 94c6fd1f-9e74-420b-9d25-61b37953b838 2024-11-05 Warnings Exact identifier application number: M017 Alocane Max LIDOCAINE HYDROCHLORIDE AND BENZALKONIUM CHLORIDE Quest Products LLC 0a35ac19-6883-a733-e063-6294a90ad22d 2024-11-05 Warnings Exact identifier application number: M017 Alocane Plus LIDOCAINE HYDROCHLORIDE AND BENZALKONIUM CHLORIDE Quest Products, Inc. cfe8114b-df65-064b-e053-2a95a90a33f6 2024-11-05 Warnings Exact identifier application number: M017 Alocane Botanicals LIDOCAINE HYDROCHLORIDE Quest Products, LLC. 02a8e5c7-56f4-eb0d-e063-6294a90a80cd 2024-11-05 Warnings Exact identifier application number: M017 Antibacterial Lidocaine Wound Gel BENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE ASO LLC cb9505b7-222d-3a24-e053-2a95a90a0b64 2024-11-05 Warnings Exact identifier application number: M017 ndc (package): 51142-652-28 ndc (product): 51142-652 ndc11 (package): 51142065228 TopCare Pain Relieving Analgesic LIDOCAINE HYDROCHLORIDE Topco Associates LLC 6b4783e0-1987-4838-9e8c-b95426d62b28 2024-11-05 Warnings Exact identifier application number: M017 Eagle Green Balm CAMPHOR MENTHOL Borden Company (Private) Limited 6f7a796b-a31c-0e60-e053-2a91aa0a022b 2024-11-04 Warnings Exact identifier application number: M017 Muscular Balm CAPSAICIN MENTHOL METHYL SALICYLATE Borden Company (Private) Limited ed79f14e-6b3d-4bf2-9c34-d019c1ba2582 2024-11-04 Warnings Exact identifier application number: M017 Hydrocortisone with Aloe HYDROCORTISONE A-S Medication Solutions 3e0aed2b-fee1-4a0c-a3d2-72cd2b3008e3 2024-11-04 Warnings Exact identifier application number: M017 Walgreens Ice Blue Pain Relieving Topical Analgesic MENTHOL, UNSPECIFIED FORM Walgreen Company 1c0ee442-ffd2-4f6c-aab2-f70e295378ad 2024-11-04 Warnings Exact identifier application number: M017 Walgreen Cool n Heat Maximum Strength Pain Relieving MENTHOL, UNSPECIFIED FORM Walgreen Company d5c79476-dde8-4a85-8878-bc2ac3a3d70b 2024-11-04 Warnings Exact identifier application number: M017 LIDOCAINE LIDOCAINE STRATUS PHARMACEUTICALS INC 87a4f559-a4f6-4b9f-98de-b55b073a11c6 2024-11-01 Warnings Exact identifier application number: M017 Walgreens Nerve Pain Relieving Topical Analgesic LIDOCAINE HYDROCHLORIDE AND MENTHOL, UNSPECIFIED FORM Walgreen Company 83849eca-e02f-4b43-b3a7-b25e987e08a8 2024-10-31 Warnings Exact identifier application number: M017 Sanar Naturals Arnica White CAMPHOR Sanvall Enterprises, Inc 192039a2-aed6-821b-e063-6394a90a7f29 2024-10-31 Warnings Exact identifier application number: M017 Sanar Naturals Arnica Reforzada CAMPHOR Sanvall Enterprises, Inc 1921a4b1-cd36-195e-e063-6294a90a8793 2024-10-31 Warnings Exact identifier application number: M017 Sanar Naturals Arnica Pain Releiving Roll On with Camphor CAMPHOR Sanvall Enterprises, Inc 173db0e2-611f-55b9-e063-6394a90ac987 2024-10-31 Warnings Exact identifier application number: M017
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 51142-652-28 51142065228 1 TUBE in 1 CARTON (51142-652-28) / 28 mL in 1 TUBE 1 tube 2019-10-28 0000-00-00 No No Current