Home NDC 68229-407 Alocane Max
Product NDC 68229-407
11-digit product format 682290407
Labeler code 68229
Product ID 68229-407_262e192e-cfcc-6344-e063-6294a90af4c5
Type HUMAN OTC DRUG
Nonproprietary name Lidocaine Hydrochloride and Benzalkonium Chloride
Dosage form LIQUID
Route TOPICAL
Labeler Quest Products LLC
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-11-15
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 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 Max
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 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 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 111 of 152 · 3,029 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 68229-407-01 68229040701 3 mL in 1 POUCH 3 ml Historical 68229-407-02 68229040702 10 POUCH in 1 CARTON (68229-407-02) / 3 mL in 1 POUCH (68229-407-01) 10 pouch 2023-11-15 No No Current 68229-407-03 68229040703 12 POUCH in 1 CARTON (68229-407-03) / 3 mL in 1 POUCH (68229-407-01) 12 pouch 2023-11-15 No No Current