Home NDC 68229-300 Alocane Plus
Product NDC 68229-300
11-digit product format 682290300
Labeler code 68229
Product ID 68229-300_3a24cc92-30d8-d5f1-e063-6294a90a537e
Type HUMAN OTC DRUG
Nonproprietary name Lidocaine Hydrochloride and Benzalkonium Chloride
Dosage form GEL
Route TOPICAL
Labeler Quest Products LLC
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-05-01
Substance LIDOCAINE HYDROCHLORIDE; BENZALKONIUM CHLORIDE
Active strength 4; .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
Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 14 matching rows.
View current auxiliary records. · View the auxiliary file history.
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 Alocane Plus
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength LIDOCAINE HYDROCHLORIDE 4 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 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2375042 Internal RxNorm lookup 2587646 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded Benzalkonium Chloride ACTIVE INGREDIENT F5UM2KM3W7 ALOCANE PLUS (LIDOCAINE HYDROCHLORIDE AND BENZALKONIUM CHLORIDE) OINTMENT [QUEST PRODUCTS, INC.] 1 Lidocaine Hydrochloride ACTIVE INGREDIENT V13007Z41A ALOCANE PLUS (LIDOCAINE HYDROCHLORIDE AND BENZALKONIUM CHLORIDE) OINTMENT [QUEST PRODUCTS, INC.] 1 Benzalkonium ACTIVE MOIETY 7N6JUD5X6Y ALOCANE PLUS (LIDOCAINE HYDROCHLORIDE AND BENZALKONIUM CHLORIDE) OINTMENT [QUEST PRODUCTS, INC.] 1 Lidocaine ACTIVE MOIETY 98PI200987 ALOCANE PLUS (LIDOCAINE HYDROCHLORIDE AND BENZALKONIUM CHLORIDE) OINTMENT [QUEST PRODUCTS, INC.] 1 .Alpha.-Tocopherol Acetate INACTIVE INGREDIENT 9E8X80D2L0 ALOCANE PLUS (LIDOCAINE HYDROCHLORIDE AND BENZALKONIUM CHLORIDE) OINTMENT [QUEST PRODUCTS, INC.] 1 Aloe Vera Leaf INACTIVE INGREDIENT ZY81Z83H0X ALOCANE PLUS (LIDOCAINE HYDROCHLORIDE AND BENZALKONIUM CHLORIDE) OINTMENT [QUEST PRODUCTS, INC.] 1 Caprylyl Glycol INACTIVE INGREDIENT 00YIU5438U ALOCANE PLUS (LIDOCAINE HYDROCHLORIDE AND BENZALKONIUM CHLORIDE) OINTMENT [QUEST PRODUCTS, INC.] 1 Chlorphenesin INACTIVE INGREDIENT I670DAL4SZ ALOCANE PLUS (LIDOCAINE HYDROCHLORIDE AND BENZALKONIUM CHLORIDE) OINTMENT [QUEST PRODUCTS, INC.] 1 Dimethyl Isosorbide INACTIVE INGREDIENT SA6A6V432S ALOCANE PLUS (LIDOCAINE HYDROCHLORIDE AND BENZALKONIUM CHLORIDE) OINTMENT [QUEST PRODUCTS, INC.] 1 Hydroxyethyl Cellulose (5500 MPA.S AT 2%) INACTIVE INGREDIENT M825OX60H9 ALOCANE PLUS (LIDOCAINE HYDROCHLORIDE AND BENZALKONIUM CHLORIDE) OINTMENT [QUEST PRODUCTS, INC.] 1 Phenoxyethanol INACTIVE INGREDIENT HIE492ZZ3T ALOCANE PLUS (LIDOCAINE HYDROCHLORIDE AND BENZALKONIUM CHLORIDE) OINTMENT [QUEST PRODUCTS, INC.] 1 Propanediol INACTIVE INGREDIENT 5965N8W85T ALOCANE PLUS (LIDOCAINE HYDROCHLORIDE AND BENZALKONIUM CHLORIDE) OINTMENT [QUEST PRODUCTS, INC.] 1 Water INACTIVE INGREDIENT 059QF0KO0R ALOCANE PLUS (LIDOCAINE HYDROCHLORIDE AND BENZALKONIUM CHLORIDE) OINTMENT [QUEST PRODUCTS, INC.] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 68229-300 ALOCANE PLUS (LIDOCAINE HYDROCHLORIDE AND BENZALKONIUM CHLORIDE) GEL [QUEST PRODUCTS, INC.] 9 Current NDC, Legacy NDC, 5 package rows 20240110_24538037-1d74-48a0-b909-98ecc57651fe.zip 68229-300 ALOCANE PLUS (LIDOCAINE HYDROCHLORIDE AND BENZALKONIUM CHLORIDE) GEL [QUEST PRODUCTS LLC] 7 Current NDC, Legacy NDC, 2 package rows 20241107_b3ec09b9-7511-0895-e053-2a95a90a7840.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 102 of 151 · 3,020 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Pain Relief Medicated CAMPHOR MENTHOL METHYL SALICYTATE RITE AID CORPORATION 60895211-69f3-478b-a33f-1c2071f62950 2025-01-16 Warnings Exact identifier application number: M017 Elgin Pain Relief MENTHOL Eco-Logics, Inc. 70eda21e-e566-42f4-9a49-b0d3ad000652 2025-01-16 Warnings Exact identifier application number: M017 Curist Lidocaine Patch Maximum Strength LIDOCAINE Little Pharma, Inc. e574c188-cc65-287d-e053-2995a90a5972 2025-01-16 Warnings Exact identifier application number: M017 Equate Hydrocortisone Topical HYDROCORTISONE WalMart 1f64555d-f77e-4a83-b222-fdb3ed7d8853 2025-01-16 Warnings Exact identifier application number: M017 Equate Hydrocortisone HYDROCORTISONE WalMart f5c32b4a-1159-4b7a-b8ac-256d53020dc2 2025-01-16 Warnings Exact identifier application number: M017 Lidocaine Pain Relief Gel-Patch LIDOCAINE Guangzhou Zhupuyou E-commerce Co., Ltd 296fcc36-563f-19ca-e063-6394a90ab3ae 2025-01-15 Warnings Exact identifier application number: M017 K19 RELIEF MENTHOL K19 LLC e2e1ca96-1ae8-4c99-b8de-ce26754292f9 2025-01-15 Warnings Exact identifier application number: M017 Anecream LIDOCAINE 4% Focus Health Group 2d7706e2-7363-4047-96cb-85b718277e8c 2025-01-15 Warnings Exact identifier application number: M017 Boroleum CAMPHOR, MENTHOL, WHITE PETROLATUM Reliable 1 Laboratories 846568af-0fdd-a80e-e053-2a91aa0a9c9e 2025-01-15 Warnings Exact identifier application number: M017 LidoPro Pain Relief CAPSAICIN AND LIDOCAINE Advanced Rx of Tennessee, LLC 27d5997b-1cc2-41c2-e063-6394a90ac74a 2025-01-15 Warnings Exact identifier application number: M017 Pain Relief Patch 4% Lidocaine LIDOCAINE Reliable 1 Laboratories LLC 2b624763-c310-63d9-e063-6394a90a1928 2025-01-15 Warnings Exact identifier application number: M017 Cannarelief 1000mg MENTHOL Carolina Cannabis Creations LLC 01e2ae1a-c969-6dd2-e063-6394a90a9d9e 2025-01-15 Warnings Exact identifier application number: M017 Healing Hand Cream 2000mg MENTHOL Carolina Cannabis Creations LLC 01f8795b-9f95-c793-e063-6394a90a8330 2025-01-15 Warnings Exact identifier application number: M017 CBD Clinic Deep-Rub Pain Relief - Level 5 CAMPHOR, MENTHOL ABACUS HEALTH PRODUCTS, INC. 31e2e5cd-d33e-f058-e063-6394a90af7d2 2025-01-14 Warnings Exact identifier application number: M017 Meijer Odor Free Analgesic Pain Relieving Topical Analgesic LIDOCAINE HYDROCHLORIDE Meijer Distribution, Inc 6288efea-f636-4eea-bb9f-78aa2f9af54a 2025-01-14 Warnings Exact identifier application number: M017 IKONIK TONIK LIDOCAINE HYDROCHLORIDE IKONIK CARE, LLC 122fdfe8-b5fa-46d1-9fd9-3df9887ed320 2025-01-14 Warnings Exact identifier application number: M017 elp essential MANTECA DE UBRE METHYL SALICYLATE, CAMPHOR Miramar Cosmetics, Inc DBA Miramar Lab c3964dfe-17fe-4d89-a4c4-cf500f982259 2025-01-13 Warnings Exact identifier application number: M017 Methylten METHYL SALICYLATE 10% Puretek Corporation 28f4093f-803f-0e70-e063-6294a90a98a4 2025-01-13 Warnings Exact identifier application number: M017 Refill Bundle 7 Large Office BENZALKONIUM CHLORIDE CMC Group, Inc. 6620a8f3-098d-d045-e053-2a91aa0a0d94 2025-01-13 Warnings Exact identifier application number: M017 Jakwork Numbing Cream NUMBING CREAM Guangzhou Zanming Trading Co., Ltd. 2ba1de83-494a-6c54-e063-6294a90a9b2d 2025-01-13 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 68229-300-01 68229030001 3.55 mL in 1 DOSE PACK 3.55 ml Historical 68229-300-02 68229030002 50 DOSE PACK in 1 BOX (68229-300-02) > 3.55 mL in 1 DOSE PACK (68229-300-01) 50 dose pack 2013-12-11 0000-00-00 No No Current 68229-300-03 68229030003 1 TUBE in 1 CARTON (68229-300-03) / 59 mL in 1 TUBE 1 tube 2020-03-01 0000-00-00 No No Current 68229-300-04 68229030004 946 mL in 1 BOTTLE, PUMP (68229-300-04) 946 ml 2021-07-09 0000-00-00 No No Current 68229-300-05 68229030005 3.55 mL in 1 DOSE PACK 3.55 ml Historical 68229-300-06 68229030006 48 DOSE PACK in 1 CARTON (68229-300-06) > 3.55 mL in 1 DOSE PACK (68229-300-05) 48 dose pack 2020-11-12 0000-00-00 No No Current