Forticept Wounds and Burns Hydrogel

Product NDC: 72127-0803
11-digit product format: 721270803
Labeler code: 72127
Product ID: 72127-0803_3b775197-f88c-4e50-a12d-c44925706e8b
Type: HUMAN OTC DRUG
Nonproprietary name: BENZETHONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE
Dosage form: GEL
Route: TOPICAL
Labeler: Lidan, inc.
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2020-05-06
Substance: BENZETHONIUM CHLORIDE; LIDOCAINE
Active strength: .001; .04 kg/kg; kg/kg
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.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Code	Status	Snapshot	Source SHA-256
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	72127-0803-0	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	72127-0803-1	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	72127-0803-0	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	72127-0803-1	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	72127-0803-0	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	72127-0803-1	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	72127-0803-0	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	72127-0803-1	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	72127-0803-1	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	72127-0803-0	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	72127-0803-1	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	72127-0803-0	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	72127-0803-1	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	72127-0803-0	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`

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: Forticept Wounds and Burns Hydrogel
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
BENZETHONIUM CHLORIDE	.001 kg/kg
LIDOCAINE	.04 kg/kg

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
PH41D05744	Internal UNII lookup
98PI200987	Internal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
c6f58b63-9838-4ff4-8b1a-de2d41d6cf5f	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDC	Effective	Related label
72127-0803-0	2025-03-25	Forticept Wounds and Burns Hydrogel
72127-0803-1	2025-03-25	Forticept Wounds and Burns Hydrogel
72127-0803-0	2025-01-30	Forticept Wounds and Burns Hydrogel
72127-0803-1	2025-01-30	Forticept Wounds and Burns Hydrogel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
72127-0803-0	Forticept Wounds and Burns Hydrogel	0.114 kg in 1 TUBE	GEL	0.114		5
72127-0803-1	Forticept Wounds and Burns Hydrogel	0.085 kg in 1 TUBE	GEL	0.085		5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72127-0803	FORTICEPT WOUNDS AND BURNS HYDROGEL (BENZETHONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE) GEL [LIDAN, INC.]	5	Current NDC, Legacy NDC, 2 package rows	20250327_c6f58b63-9838-4ff4-8b1a-de2d41d6cf5f.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 3 of 156 · 3,115 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
CVS Pain Relief Lidocaine XL	LIDOCAINE	CVS Pharmacy	4aa286e3-e274-8095-e063-6394a90ae871	2026-08-26	Warnings	Exact identifier application number: M017
TERAPIA DE DIA Y NOCHE	PAIN RELIEVING PATCH	DW SUPPORT LLC	59f44135-865b-9d7d-e063-6294a90a9dd9	2026-08-26	Warnings	Exact identifier application number: M017
Calamine Plus	CALAMINE, PRAMOXINE HYDROCHLORIDE	Kroger Company	44fdd5a4-3cac-15e5-e063-6294a90adb52	2026-08-26	Warnings	Exact identifier application number: M017
Lidocaine Pain Relief	LIDOCAINE	Cardinal Health, 110 dba LEADER	025d508b-ec4f-466c-b3e8-ba9b18d07b46	2026-08-26	Warnings	Exact identifier application number: M017
Inknows Lidocaine Pain Relief Gel-Patch	LIDOCAINE PAIN RELIEF GEL-PATCH	Henan Enokon Medical Instrument Co., Ltd.	59eb9c12-9e00-0171-e063-6394a90a8342	2026-08-25	Warnings	Exact identifier application number: M017
Lidomar	LIDOMAR	Oncora Pharma, LLC	215bfdca-60bf-480b-b02e-902de52fe5e8	2026-08-25	Warnings	Exact identifier application number: M017
Hydrocortisone	HYDROCORTISONE	Amazon.com Services LLC	5f87d7fb-f258-48b0-8b60-1055e22ebd71	2026-08-25	Warnings	Exact identifier application number: M017
HEEL PAIN RELIEF ROLL-ON	LIDOCAINE AND MENTHOL	Guangzhou Liuquanmiao Import & Export Trade Co., Ltd.	59c7e13f-b9ea-023a-e063-6294a90a79e0	2026-08-24	Warnings	Exact identifier application number: M017
KNEE PAIN RELIEF ROLL-ON	LIDOCAINE AND MENTHOL	Guangzhou Liuquanmiao Import & Export Trade Co., Ltd.	59c8b33a-7d4f-2c6e-e063-6394a90a7929	2026-08-24	Warnings	Exact identifier application number: M017
Bovonte Numbing Cream	NUMBING CREAM	Guangzhou Jingliang Cosmetics Co., Ltd.	5958cc29-c449-56a7-e063-6394a90a960b	2026-08-24	Warnings	Exact identifier application number: M017
HUSTLE BUTTER NUMBING	LIDOCAINE HYDROCHLORIDE	H.B.D. D.I.S.T. INC.	d7dfb312-6c80-4a2d-b8b2-d9891cb0b74e	2026-08-24	Warnings	Exact identifier application number: M017
JELVOXA NECK PAIN RELIEVING	MENTHOL	Wuhan Ruihengjie Technology Co., Ltd.	59a3d60a-26b5-e6a6-e063-6294a90a42bd	2026-08-22	Warnings	Exact identifier application number: M017
JELVOXA DMSO	CAMPHOR CAPSAICIN MENTHOL	Wuhan Ruihengjie Technology Co., Ltd.	59a43e2c-d258-34b5-e063-6394a90a09bf	2026-08-22	Warnings	Exact identifier application number: M017
Capsaicin 0.035 Percent	CAPSAICIN	Preferred Pharmaceuticals Inc.	0fabc025-4208-45f5-b3c2-543ae3a2df41	2026-08-21	Warnings	Exact identifier application number: M017
Claravie	HYDROCORTISONE ACETATE	Gentell LLC	598d224b-d12e-89bf-e063-6394a90a84dc	2026-08-21	Warnings	Exact identifier application number: M017
ETERNAL SPIRIT BEAUTY PAINLESS PAIN RELIEVING	MENTHOL, CAMPHOR	Worldwide Cosmetics, Inc	3b8c2419-7a78-2731-e054-00144ff8d46c	2026-08-21	Warnings	Exact identifier application number: M017
PARCHE FRIO	METHYL SALICYLATE, MENTHOL, AND CAMPHOR PATCH	DW SUPPORT LLC	5970a6f7-b273-9bb1-e063-6394a90afc79	2026-08-21	Warnings	Exact identifier application number: M017
Enokon Lidocaine Pain Relief Patch	LIDOCAINE PAIN RELIEF PATCH	Henan Enokon Medical Instrument Co., Ltd.	5976e667-e506-1d11-e063-6394a90a6809	2026-08-20	Warnings	Exact identifier application number: M017
MQUPIN TIGER Patch	TIGER PATCH	Zhengzhou Miaoqi Medical Technology Co., Ltd.	5977cbb5-94c7-cb24-e063-6294a90a2e07	2026-08-20	Warnings	Exact identifier application number: M017
MQUPIN Nicotine Patches	NICOTINE PATCHES	Zhengzhou Miaoqi Medical Technology Co., Ltd.	5978258a-549e-50e6-e063-6394a90a3d86	2026-08-20	Warnings	Exact identifier application number: M017

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
PH41D05744	BENZETHONIUM CHLORIDE	121-54-0	BENZETHONIUM CHLORIDE
98PI200987	LIDOCAINE	137-58-6	LIDOCAINE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
72127-0803-0	72127080300	.114 kg in 1 TUBE (72127-0803-0)	2020-05-06	0000-00-00	No	No	Current
72127-0803-1	72127080301	.085 kg in 1 TUBE (72127-0803-1)	2021-02-18	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Forticept Wounds and Burns Hydrogel	Lidan, inc. \| Cosco International, Inc.	2025-03-25	HUMAN OTC DRUG LABEL	5