Home NDC 68229-406 Alocane Max
Product NDC 68229-406
11-digit product format 682290406
Labeler code 68229
Product ID 68229-406_4de08098-5946-ba6e-e063-6294a90a8dbe
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 2027-12-31
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 2027-12-31 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# DailyMed Package Descriptions# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 68229-406 ALOCANE MAX (LIDOCAINE HYDROCHLORIDE AND BENZALKONIUM CHLORIDE) GEL [QUEST PRODUCTS LLC] 4 Current NDC, 11 package rows 20250212_0a33f9a9-1fdc-7cdf-e063-6294a90adca1.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 18 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 Sample Exclude flag Status 68229-406-01 68229040601 75 mL in 1 TUBE 75 ml Historical 68229-406-02 68229040602 1 TUBE in 1 CARTON (68229-406-02) / 75 mL in 1 TUBE (68229-406-01) 1 tube 2023-11-15 No No Current 68229-406-03 68229040603 118 mL in 1 TUBE 118 ml Historical 68229-406-05 68229040605 1 TUBE in 1 CARTON (68229-406-05) / 118 mL in 1 TUBE (68229-406-03) 1 tube 2023-11-15 No No Current 68229-406-06 68229040606 3.4 mL in 1 PACKET 3.4 ml Historical 68229-406-07 68229040607 24 PACKET in 1 CARTON (68229-406-07) / 3.4 mL in 1 PACKET (68229-406-06) 24 packet 2023-11-15 No No Current 68229-406-08 68229040608 110 mL in 1 TUBE 110 ml Historical 68229-406-09 68229040609 1 TUBE in 1 CARTON (68229-406-09) / 110 mL in 1 TUBE (68229-406-08) 1 tube 2025-02-10 No No Current 68229-406-10 68229040610 59 mL in 1 TUBE 59 ml Historical 68229-406-11 68229040611 1 TUBE in 1 CARTON (68229-406-11) / 59 mL in 1 TUBE (68229-406-10) 1 tube 2025-12-04 No No Current 68229-406-85 68229040685 251.4 mL in 1 TUBE (68229-406-85) 251.4 ml 2025-12-15 No No Current