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

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 3 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Source date
excluded package	package	68229-300	68229-300-06	D	Discontinued by firm	2026-10-21
excluded package	package	68229-300	68229-300-02	D	Discontinued by firm	2026-10-21
excluded package	package	68229-300	68229-300-04	D	Discontinued by firm	2026-10-21

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.

Captured / source date, Package NDC, Snapshot table
Captured / source date	Package NDC	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	68229-300-04	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	68229-300-02	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	68229-300-04	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	68229-300-02	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	68229-300-02	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	68229-300-02	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	68229-300-02	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	68229-300-02	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	68229-300-02	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	68229-300-02	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	68229-300-02	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	68229-300-02	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	68229-300-02	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	68229-300-02	`557ba5c1ecfa…`	`9c80585c8c6e…`

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.

Identifier, FDA.report destination table
Identifier	FDA.report destination
b3ec09b9-7511-0895-e053-2a95a90a7840	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
070fbed5-7088-434a-a7ce-f2a64d8d40ac	Product name	2	20260107
bee66ce1-adb7-9d3b-67d9-582e4c54e80f	Product name	5	20250819
860a93dc-4863-49cc-b284-6bbe8191bc48	Product name	4	20250214
eaba870a-6a9d-442e-8643-87b3f558a451	Product name	1	20250117
9b4cf230-fd05-41d5-98c6-5db9ecb27b86	Product name	1	20230117
7d755fa1-1087-4dcd-98f0-6d4bba479a57	Product name	3	20210602
aed701d5-9c75-dfaf-7154-cde46179faea	Product name	9	20200313
fa8b5901-e681-426f-82fe-54f6d81ec698	Product name	4	20180619
332d03e4-aa24-4b11-841a-02bf41081920	Product name	1	20171221
c08ab52f-2fc8-4409-9d9f-ed8edc0bd070	Product name	1	20171221
68ed98f8-24c2-44a0-944a-6d36e82ce25a	Product name	1	20141222
1cd42bc2-a430-c72b-636d-991b235fbf80	Product name	1	20140508
49fa150c-f0de-cce7-3d9c-993ed81c5698	Product name	1	20140508
4d7ae718-ed00-bae8-2abe-9eaec1eef7ff	Product name	1	20140508
9137811f-f279-8640-5aeb-99fa2145d64d	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
68229-300-02	2020-02-03	C162847	48780-1	9d75b9d1-2b47-f424-e053-dadaa90a57ce	Alocane ® Plus
68229-300-02	2020-01-31	C162847	48780-1	9d75b9d1-2b47-f424-e053-dadaa90a57ce	Alocane ® Plus

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
68229-300-01	Alocane Plus	3.55 mL in 1 DOSE PACK	GEL	3.55	10
68229-300-02	Alocane Plus	50 in 1 BOX	GEL	50	10
68229-300-03	Alocane Plus	1 in 1 CARTON	GEL	1	10
68229-300-03	Alocane Plus	59 mL in 1 TUBE	GEL	59	10
68229-300-04	Alocane Plus	946 mL in 1 BOTTLE, PUMP	GEL	946	10
68229-300-05	Alocane Plus	3.55 mL in 1 DOSE PACK	GEL	3.55	8
68229-300-06	Alocane Plus	48 in 1 CARTON	GEL	48	8

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
68229-300-01	EA - Each	68229-300	379cbe87-939f-4066-8e28-789c4c3430db	1	2021-01-08
68229-300-02	EA - Each	68229-300	b520af95-ef09-4734-9392-dcb3d85fe981	1	2021-01-08
68229-300-03	ML - Milliliter	68229-300	27207190-a638-4f5a-b3df-27cde1c29d3b	1	2021-09-07
68229-300-04	ML - Milliliter	68229-300	74748392-6b14-42fc-8c52-9340ed8a8bb3	1	2021-09-07
68229-300-05	ML - Milliliter	68229-300	e75b92b2-0797-472a-8c2e-1f676e76b8ff	2	2022-02-07
68229-300-06	ML - Milliliter	68229-300	110ad54a-6f0b-4007-9433-4a41ec8d3543	2	2022-02-07

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
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 66 of 152 · 3,029 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
MENTHOL AND METHYL SALICYLATE	ELECTRIC MEDICATED BALM ULTRA STRENGTH	FEI FAH MEDICAL MANUFACTURING PTE LTD	91e6d3b9-25bb-4015-9d96-bd27f93e5ada	2025-11-10	Warnings	Exact identifier application number: M017
E MEI SHAN MEDICATED	CAMPHOR, MENTHOL	Zhejiang Dingtai Pharmaceutical Co., Ltd	bda1e7c1-42df-4126-a512-80f843b07fd0	2025-11-10	Warnings	Exact identifier application number: M017
EXTRA STRENGTH HUA TUO PAIN RELIEVING	CAMPHOR AND MENTHOL	Zhejiang Dingtai Pharmaceutical Co., Ltd	9850754b-ac94-4ec6-b75a-8096e5ac9456	2025-11-10	Warnings, Adverse reactions	Exact identifier application number: M017
TONG FENG DING PAIN RELIEF	CAMPHOR AND MENTHOL	Zhejiang Dingtai Pharmaceutical Co., Ltd	fe87b864-b3ee-4a4b-8e5a-e1ee6493de0d	2025-11-10	Warnings, Adverse reactions	Exact identifier application number: M017
Solstice Pain Relieving	CAMPHOR, MENTHOL, METHYL SALICYLATE	MADISON ONE ACME INC	5ef90782-8201-47d1-b57f-f032d4c9b06a	2025-11-10	Warnings, Adverse reactions	Exact identifier application number: M017
Solstice Pain Relieving	CAMPHOR, MENTHOL, METHYL SALICYLATE	MADISON ONE ACME INC	1388ab3a-c26f-427d-898d-0d88411a5fba	2025-11-10	Warnings, Adverse reactions	Exact identifier application number: M017
Solstice Capsaicin Patch Hot	CAPSAICIN	MADISON ONE ACME INC	f74db6e0-853a-4eb3-a4b5-9da2cd3d95cf	2025-11-10	Warnings, Adverse reactions	Exact identifier application number: M017
Lung Choy Shung Pain Relief Liquid	MENTHOL AND CAMPHOR	MADISON ONE ACME INC	4842c6ec-7823-4f6b-afc4-258fce2c2391	2025-11-10	Warnings, Adverse reactions	Exact identifier application number: M017
701 DIEDA ZHENGTONG YAOGAO MEDICATED	CAMPHOR AND MENTHOL	MADISON ONE ACME INC	115041ff-5046-4ca4-b54b-5652037e74bd	2025-11-10	Warnings, Adverse reactions	Exact identifier application number: M017
EXTRA STRENGTH HUA TUO PAIN RELIEF	CAMPHOR AND MENTHOL	MADISON ONE ACME INC	0f269a41-4b56-4e22-b9cb-17d99bf76a57	2025-11-10	Warnings, Adverse reactions	Exact identifier application number: M017
ZANG HONG HUA PAIN RELIEVING	CAMPHOR, CAPSAICIN, AND METHYL SALICYLATE	MADISON ONE ACME INC	e0a8811c-07cf-4dee-a0e5-13b8af1b27b6	2025-11-10	Warnings, Adverse reactions	Exact identifier application number: M017
NECK AND LUMBAR PAIN RELIEVING BALM	CAMPHOR, MENTHOL, METHYL SALICYLATE	MADISON ONE ACME INC	d06f0650-a5f6-4bc1-a70b-b0fc16968fa9	2025-11-10	Warnings, Adverse reactions	Exact identifier application number: M017
SHU JIN HUO LUO PAIN RELIEVING	CAMPHOR, MENTHOL, METHYL SALICYLATE	MADISON ONE ACME INC	ccb6740d-3399-4a2b-ae65-15ca557ba83b	2025-11-10	Warnings, Adverse reactions	Exact identifier application number: M017
GuruNanda Pain Relief	LIDOCAINE HYDROCHLORIDE	GuruNanda, LLC.	3ab6a133-8dca-e14e-e063-6394a90a85e7	2025-11-10	Warnings	Exact identifier application number: M017
HUO LUO PAIN RELIEVING	CAMPHOR, MENTHOL, METHYL SALICYLATE	MADISON ONE ACME INC	65581716-5a2c-4ee8-816d-00caed7b95b4	2025-11-10	Warnings, Adverse reactions	Exact identifier application number: M017
JOSEPHS LION PAIN RELIEVING	CAMPHOR, MENTHOL, METHYL SALICYLATE	MADISON ONE ACME INC	69b88e21-2001-4fb2-b6eb-17f2d6e0ef2e	2025-11-10	Warnings, Adverse reactions	Exact identifier application number: M017
QIAN LI ZHUI FENG PAIN RELIEVING	CAMPHOR, MENTHOL, AND METHYL SALICYLATE	MADISON ONE ACME INC	03a4fb7c-2328-409d-99c8-cbcf2b4a451f	2025-11-10	Warnings, Adverse reactions	Exact identifier application number: M017
WU YANG BRAND PAIN RELIEVING MEDICATED	MENTHOL AND CAMPHOR	MADISON ONE ACME INC	05c6b95a-aeb6-4234-97c7-8d77eccb38d8	2025-11-10	Warnings	Exact identifier application number: M017
HEI GUI PAIN RELIEVING	CAMPHOR AND METHYL SALICYLATE	MADISON ONE ACME INC	4140c404-edab-4923-941d-f74125e943a9	2025-11-10	Warnings, Adverse reactions	Exact identifier application number: M017
E MEI SHAN MEDICATED	CAMPHOR AND MENTHOL	MADISON ONE ACME INC	ddcc814e-fcc4-4232-9ab4-826b8aac35f0	2025-11-10	Warnings, Adverse reactions	Exact identifier application number: M017

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
V13007Z41A	LIDOCAINE HYDROCHLORIDE	6108-05-0	LIDOCAINE HYDROCHLORIDE
F5UM2KM3W7	BENZALKONIUM CHLORIDE	8001-54-5	BENZALKONIUM CHLORIDE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
2587646	ALOCANE plus 4 % / 0.13 % Topical Gel	PSN	24538037-1d74-48a0-b909-98ecc57651fe	10
2375042	benzalkonium chloride 0.13 % / lidocaine hydrochloride 4 % Topical Gel	PSN	24538037-1d74-48a0-b909-98ecc57651fe	10
2587646	benzalkonium chloride 0.0013 MG/MG / lidocaine hydrochloride 0.04 MG/MG Topical Gel [Alocane Plus]	SBD	24538037-1d74-48a0-b909-98ecc57651fe	10
2375042	benzalkonium chloride 0.0013 MG/MG / lidocaine hydrochloride 0.04 MG/MG Topical Gel	SCD	24538037-1d74-48a0-b909-98ecc57651fe	10
2587646	Alocane Plus (benzalkonium chloride 0.13 % / lidocaine hydrochloride 4 % ) Topical Gel	SY	24538037-1d74-48a0-b909-98ecc57651fe	10
2375042	benzalkonium chloride 0.13 % / lidocaine hydrochloride 4 % Topical Gel	SY	24538037-1d74-48a0-b909-98ecc57651fe	10
2587646	ALOCANE plus 4 % / 0.13 % Topical Gel	PSN	b3ec09b9-7511-0895-e053-2a95a90a7840	8
2375042	benzalkonium chloride 0.13 % / lidocaine hydrochloride 4 % Topical Gel	PSN	b3ec09b9-7511-0895-e053-2a95a90a7840	8
2587646	benzalkonium chloride 0.0013 MG/MG / lidocaine hydrochloride 0.04 MG/MG Topical Gel [Alocane Plus]	SBD	b3ec09b9-7511-0895-e053-2a95a90a7840	8
2375042	benzalkonium chloride 0.0013 MG/MG / lidocaine hydrochloride 0.04 MG/MG Topical Gel	SCD	b3ec09b9-7511-0895-e053-2a95a90a7840	8
2587646	Alocane Plus (benzalkonium chloride 0.13 % / lidocaine hydrochloride 4 % ) Topical Gel	SY	b3ec09b9-7511-0895-e053-2a95a90a7840	8
2375042	benzalkonium chloride 0.13 % / lidocaine hydrochloride 4 % Topical Gel	SY	b3ec09b9-7511-0895-e053-2a95a90a7840	8

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

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Alocane ® Plus	Quest Products LLC	2025-12-04	HUMAN OTC DRUG LABEL	8
Alocane ® Plus	Quest Products, Inc. \| Fill Tech USA	2025-07-17	HUMAN OTC DRUG LABEL	10