Home NDC 68229-201 Alocane Emergency Burn
Product NDC 68229-201
11-digit product format 682290201
Labeler code 68229
Product ID 68229-201_262e0e1d-21b6-be5e-e063-6394a90ab0aa
Type HUMAN OTC DRUG
Nonproprietary name Lidocaine Hydrochloride
Dosage form GEL
Route TOPICAL
Labeler Quest Products, LLC.
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-03-01
Substance LIDOCAINE HYDROCHLORIDE
Active strength 4 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 · 21 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 Emergency Burn
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength LIDOCAINE HYDROCHLORIDE 4 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination V13007Z41A Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1010077 Internal RxNorm lookup 1875237 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 68229-201 ALOCANE EMERGENCY BURN (LIDOCAINE HYDROCHLORIDE) GEL [QUEST PRODUCTS, LLC.] 14 Current NDC, Legacy NDC, 18 package rows 20241107_0c8e65a6-dff3-43b4-a3f1-95deb574ea89.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 146 of 152 · 3,029 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join SUPER BLUE STUFF Pain Relief Cream MENTHOL BLUE SPRING WELLNESS, L.L.C. 066a2106-2e25-4df6-9a8d-4417ba190205 2023-11-10 Warnings Exact identifier application number: M017 INVIGO FLEX Pain Relief Gel MENTHOL WYNNPHARM INC. 909e1d8c-c517-4d6a-8682-894f042c00f8 2023-11-10 Warnings Exact identifier application number: M017 ARNIMAX Penetrating Pain Relief Gel MENTHOL WYNNPHARM INC. 3a31f805-19c6-4036-a663-ebef9b212007 2023-11-10 Warnings Exact identifier application number: M017 KERA HC HYDROCORTISONE Clinical Therapeutic Solutions ac215c8f-b224-480c-9295-3a34316293ba 2023-11-10 Warnings Exact identifier application number: M017 ALO THERAPEUTIC MASSAGE PAIN RELIEVING MENTHOL, HISTAMINE DIHYDROCHLORIDE Theraplex Solutions da004500-5e48-487b-b96f-520a3094096c 2023-11-10 Warnings Exact identifier application number: M017 Osteo Bi-Flex JOINT HEALTH PAIN RELIEVING MENTHOL, METHYL SALICYLATE Rexall Sundown, LLC 55c55f1c-d2b3-6363-e054-00144ff88e88 2023-11-10 Warnings Exact identifier application number: M017 NEUROFLEX Topical Pain Relieving Liquid CAMPHOR (SYNTHETIC), MENTHOL Almark Products Inc 6da3aa84-7a01-4041-8792-a4bbf49e6e4e 2023-11-10 Warnings Exact identifier application number: M017 SMOOTH GATOR 60-second Pain Relief CAMPHOR (SYNTHETIC), MENTHOL Smooth Gator LLC 3b74b542-202f-469e-8025-4372e95e6b01 2023-11-10 Warnings Exact identifier application number: M017 Alo Therapeutic Massage MENTHOL, HISTAMINE DIHYDROCHLORIDE CMI Therapy Solutions 40f8b8d1-a20b-54b0-e054-00144ff88e88 2023-11-10 Warnings Exact identifier application number: M017 Alo Therapeutic Massage MENTHOL, HISTAMINE DIHYDROCHLORIDE CMI Therapy Solutions 40f92e71-fe2e-16f4-e054-00144ff8d46c 2023-11-10 Warnings Exact identifier application number: M017 Teeter Renew Muscles Pain Relieving METHYL SALICYLATE, MENTHOL STL International INC b90dc5b9-c31d-4770-a291-98d036ae8723 2023-11-10 Warnings Exact identifier application number: M017 SMOOTH GATOR Foot and Leg Rub CAMPHOR (SYNTHETIC), MENTHOL Smooth Gator LLC 57094238-506b-48c1-8eb9-fe904be80df0 2023-11-10 Warnings Exact identifier application number: M017 SKIN A COOL Hydrocortisone Anti-Itch HYDROCORTISONE Ana-Cool, LLC e3ea7406-e494-4038-9b28-8d0a28b4b834 2023-11-10 Warnings Exact identifier application number: M017 Teeter reNEW MUSCLES Pain Relieving METHYL SALICYLATE, MENTHOL STL International INC ebc777b0-d141-4a62-9366-d14787eaefe0 2023-11-10 Warnings Exact identifier application number: M017 FEELGOOD LAB Natural Pain Cream MENTHOL The Feel Good Lab, LLC 799d464c-aaf1-429a-877b-2a692397bb49 2023-11-10 Warnings Exact identifier application number: M017 HIGHER CONTROL Male Climax Control Lubricating BENZOCAINE Product Max Group Inc 5f5fd127-34c5-403a-aa95-c9874ae79492 2023-11-10 Warnings Exact identifier application number: M017 Alo Therapeutic Massage MENTHOL, HISTAMINE DIHYDROCHLORIDE CMI Therapy Solutions 40f93076-1f68-58e6-e054-00144ff88e88 2023-11-10 Warnings Exact identifier application number: M017 Alo Therapeutic Massage MENTHOL, HISTAMINE DIHYDROCHLORIDE CMI Therapy Solutions 40f9622e-27c7-6a5d-e054-00144ff88e88 2023-11-10 Warnings Exact identifier application number: M017 FEEL GOOD LAB Natural Pain Cream MENTHOL THE FEEL GOOD LAB, LLC 774a72b1-b719-4217-846e-7f9921fd1b16 2023-11-10 Warnings Exact identifier application number: M017 BODY ACTION PRODUCTS Climax Control Gel BENZOCAINE PRODUCT MAX GROUP INC 53e746cc-0078-4381-bf0b-9c8f98d66904 2023-11-10 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 68229-201-01 68229020101 110 mL in 1 TUBE 110 ml Historical 68229-201-02 68229020102 1 TUBE in 1 CARTON (68229-201-02) / 110 mL in 1 TUBE (68229-201-01) 1 tube 2019-03-01 0000-00-00 No No Current 68229-201-03 68229020103 110 mL in 1 BOTTLE, SPRAY (68229-201-03) 110 ml 2020-03-01 0000-00-00 No No Current 68229-201-04 68229020104 3.4 mL in 1 PACKET 3.4 ml Historical 68229-201-05 68229020105 24 PACKET in 1 CARTON (68229-201-05) / 3.4 mL in 1 PACKET (68229-201-04) 24 packet 2020-03-01 0000-00-00 No No Current 68229-201-06 68229020106 3.4 mL in 1 PACKET 3.4 ml Historical 68229-201-07 68229020107 45 PACKET in 1 CARTON (68229-201-07) / 3.4 mL in 1 PACKET (68229-201-06) 45 packet 2020-03-01 0000-00-00 No No Current 68229-201-08 68229020108 103.507 mL in 1 BOTTLE, SPRAY (68229-201-08) 103.507 ml 2020-03-01 0000-00-00 No No Current 68229-201-09 68229020109 118.294 mL in 1 TUBE 118.294 ml Historical 68229-201-10 68229020110 1 TUBE in 1 CARTON (68229-201-10) / 118.294 mL in 1 TUBE (68229-201-09) 1 tube 2019-03-01 0000-00-00 No No Current 68229-201-11 68229020111 133.081 mL in 1 BOTTLE, SPRAY (68229-201-11) 133.081 ml 2020-03-01 0000-00-00 No No Current 68229-201-12 68229020112 1 BAG in 1 KIT (68229-201-12) > 800 mL in 1 BAG (68229-201-15) 1 bag 2019-03-01 0000-00-00 No No Current 68229-201-13 68229020113 1 BAG in 1 CARTON (68229-201-13) / 800 mL in 1 BAG (68229-201-15) 1 bag 2019-03-01 0000-00-00 No No Current 68229-201-14 68229020114 946 mL in 1 BOTTLE, PUMP (68229-201-14) 946 ml 2019-03-01 0000-00-00 No No Current 68229-201-15 68229020115 800 mL in 1 BAG 800 ml Historical 68229-201-16 68229020116 124 mL in 1 BOTTLE, SPRAY (68229-201-16) 124 ml 2022-11-11 0000-00-00 No No Current 68229-201-17 68229020117 22 mL in 1 TUBE 22 ml Historical 68229-201-18 68229020118 1 TUBE in 1 CARTON (68229-201-18) / 22 mL in 1 TUBE (68229-201-17) 1 tube 2021-12-09 0000-00-00 No No Current