Home NDC 68229-407-01 NDC 68229-407-01 - Alocane Max This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
Product NDC 68229-407
Requested NDC 68229-407-01
Package NDCs from labels 68229-407-01, 68229-407-02, 68229-407-03
Manufacturer Quest Products LLC
Effective date 2024-11-05
Current FDA listing Not matched in FDA.report NDC product tables
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 68229-407-01 Alocane Max 3 mL in 1 POUCH LIQUID 3 2 68229-407-02 Alocane Max 10 in 1 CARTON LIQUID 10 2 68229-407-03 Alocane Max 12 in 1 CARTON LIQUID 12 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 68229-407 ALOCANE MAX (LIDOCAINE HYDROCHLORIDE AND BENZALKONIUM CHLORIDE) LIQUID [QUEST PRODUCTS LLC] 2 Current NDC, 3 package rows 20241107_0a35ac19-6883-a733-e063-6294a90ad22d.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 35 of 230 · 4,587 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Vita Vie Antibacterial Wash BENZALKONIUM CHLORIDE Spa De Soleil a83883b7-9b63-641b-e053-2995a90ab943 2026-04-30 Warnings Exact identifier unii: F5UM2KM3W7 Dr Lift Advanced Antibacterial Wipes BENZALKONIUM CHLORIDE Spa de Soleil af89bd25-784e-4828-e053-2995a90a8aaa 2026-04-30 Warnings Exact identifier unii: F5UM2KM3W7 Dr Lift Antibacterial Hand Wash BENZALKONIUM CHLORIDE Spa de Soleil ab9e2c3c-d422-255e-e053-2a95a90a7a22 2026-04-30 Warnings Exact identifier unii: F5UM2KM3W7 Dr Lift Antibacterial Body Scrub BENZALKONIUM CHLORIDE Spa de Soleil ab9d6c73-29c1-036a-e053-2995a90a449c 2026-04-30 Warnings Exact identifier unii: F5UM2KM3W7 KLEENEX Foam Hand Sanitizer BENZALKONIUM CHLORIDE Kimberly-Clark 1fa77ae2-b652-463d-8943-d338c591226e 2026-04-29 Warnings Exact identifier unii: F5UM2KM3W7 1438 DynaSoap ANTIBACTERIAL HAND SOAP Dynarex Corporation ab0d5f64-9168-2ea3-e053-2a95a90a321e 2026-04-29 Warnings Exact identifier unii: F5UM2KM3W7 Summit 367 Antibacterial Foam BENZALKONIUM CHLORIDE R.L. Williams Company 509f2491-ea17-86ee-e063-6394a90a5940 2026-04-29 Warnings Exact identifier unii: F5UM2KM3W7 E2 Antibacterial Foaming Skin Cleanser BENZALKONIUM CHLORIDE Betco Corporation, Ltd. aa7c24bb-cc66-3081-e053-2a95a90ada03 2026-04-29 Warnings Exact identifier unii: F5UM2KM3W7 hydrocortisone HYDROCORTISONE Padagis Israel Pharmaceuticals Ltd 2dc7f76f-f9ad-46ba-8b41-952e1c15f052 2026-04-29 Warnings Exact identifier application number: M017 anti itch HYDROCORTISONE HyVee Inc e1db3641-2e83-4fec-8394-98d0d876ce0d 2026-04-29 Warnings Exact identifier application number: M017 Eagle Brand Medicated Roll On MENTHOL, METHYL SALICYLATE PT. EAGLE INDO PHARMA 50805eee-33b3-86bd-e063-6294a90a77d8 2026-04-28 Warnings Exact identifier application number: M017 FixMySkin Healing Balm Vanilla Flavor HYDROCORTISONE Lovely Skin, Inc. 52f7a561-a0b5-4562-a588-d74fd874b83a 2026-04-28 Warnings Exact identifier application number: M017 SCOTT Antimicrobial Foam Skin Cleanser BENZALKONIUM CHLORIDE Kimberly-Clark 210f7da3-63c5-4a4b-8db0-8d6d1663751d 2026-04-28 Warnings Exact identifier unii: F5UM2KM3W7 Blue Star Medicated CAMPHOR Focus Consumer Healthcare, LLC 56df008e-a23b-4870-e054-00144ff8d46c 2026-04-27 Warnings Exact identifier application number: M017 Eagle Brand Muscle Rub MENTHOL, METHYL SALICYLATE Borden Company (Private) Limited 06cb845c-cc53-1f1d-e063-6394a90a8c01 2026-04-27 Warnings Exact identifier application number: M017 anzoon ANTISEPTIC WIPES BENZETHONIUM CHLORIDE/BENZALKONIUM CHLORIDE Shandong ACZ Biotechnology Co., Ltd. 506cd089-f9a7-d9e5-e063-6394a90af696 2026-04-27 Warnings Exact identifier unii: F5UM2KM3W7 Eagle Brand Medicated Oil Aromatic CAMPHOR, MENTHOL, METHYL SALICYLATE PT. EAGLE INDO PHARMA 0ef7c3aa-94a3-9fe9-e063-6394a90ab13d 2026-04-27 Warnings Exact identifier application number: M017 Eagle Brand Medicated Oil MENTHOL, METHYL SALICYLATE PT. EAGLE INDO PHARMA 5071f145-49f7-0855-e063-6394a90a8f26 2026-04-27 Warnings Exact identifier application number: M017 Eagle Brand Medicated Oil Refresh CAMPHOR, MENTHOL PT. EAGLE INDO PHARMA 09260c31-56a3-07aa-e063-6394a90a95fd 2026-04-27 Warnings Exact identifier application number: M017 Eagle Brand Muscle Rub MENTHOL, METHYL SALICYLATE PT. EAGLE INDO PHARMA 5072ad57-9fa7-ddba-e063-6394a90a319b 2026-04-27 Warnings Exact identifier application number: M017
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.