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 69 of 153 · 3,057 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Topcare Cold and Hot Medicated	MENTHOL	Topco Associates LLC	8739aedd-165c-5ae0-e053-2a91aa0afcd0	2025-10-31	Warnings	Exact identifier application number: M017
CVS Medicated Heat 1 ct	CAPSAICIN	CVS Pharmacy, Inc.	d41dce5b-e698-4930-8869-040b2a973f25	2025-10-31	Warnings	Exact identifier application number: M017
Coralite Medicated Heat	CAPSAICIN	United Exchange Corp.	a0b89c7e-80bc-43c4-840c-5fd567f60b21	2025-10-31	Warnings	Exact identifier application number: M017
Dragon with Arnical Pain Relief	MENTHOL	Genomma Lab USA Inc.	b4cbb7b6-cb71-9721-e053-2995a90a2b2c	2025-10-31	Warnings	Exact identifier application number: M017
Hydrocortisone Anti-Itch	HYDROCORTISONE	Universal Distribution Center LLC	186afb11-06b6-4bfa-e063-6294a90aefc6	2025-10-30	Warnings	Exact identifier application number: M017
Gemachlich ZuHause NEUROPATHY SOLID Ointment.	GEMACHLICH ZUHAUSE NEUROPATHY SOLID OINTMENT.	Guangdong Quadrant Ecological Technology Co., Ltd.	425b1b9d-c33a-05e9-e063-6394a90a97a6	2025-10-30	Warnings	Exact identifier application number: M017
Gemachlich ZuHause NEUROPATHY Spray.	GEMACHLICH ZUHAUSE NEUROPATHY SPRAY.	Guangdong Quadrant Ecological Technology Co., Ltd.	425b8259-af38-8d68-e063-6394a90a1120	2025-10-30	Warnings	Exact identifier application number: M017
Family Care Muscle and Joint	MENTHOL	United Exchange Corp.	959af9f4-7188-91a1-e053-2995a90a4665	2025-10-30	Warnings	Exact identifier application number: M017
CVS Maximum Strength Boil Relief	BENZOCAINE	CVS Pharmacy, Inc.	0761b866-af34-42bd-adc9-3d229170d01c	2025-10-30	Warnings	Exact identifier application number: M017
CVS Cold and Hot	MENTHOL	CVS Pharmacy	a44ca52d-fec8-0e8c-e053-2995a90a2e60	2025-10-30	Warnings	Exact identifier application number: M017
CVS CAPSAICIN	CAPSAICIN	CVS PHARMACY	9b551fe3-3842-482a-9042-63de5ad39884	2025-10-30	Warnings	Exact identifier application number: M017
TopCare Health Pain Relief	MENTHOL, CAMPHOR, AND METHYL SALICYLATE	Topco Associates LLC	dac364ef-6dcd-3fc6-e053-2a95a90a9bb2	2025-10-30	Warnings	Exact identifier application number: M017
Calamine Plus	CALAMINE PLUS PRAMOXINE HCL	AmerisourceBergen Drug Corporation	f161e151-4fab-2fbc-e053-2a95a90a5437	2025-10-30	Warnings	Exact identifier application number: M017
Lidocaine	BURN RELIEF	Perrigo Direct	c7b50f14-3481-9ebd-e053-2995a90afe1c	2025-10-30	Warnings	Exact identifier application number: M017
Lipoflavonoid Ear Pain Kids Relief Drops	LIPOFLAVONOID EAR PAIN KIDS RELIEF DROPS	Clarion Brands LLC	4265361b-5526-c3e0-e063-6394a90a1777	2025-10-30	Warnings	Exact identifier application number: M017
Diphenhydramine HCl and Zinc Acetate	EXTRA STRENGTH ITCH RELIEF	HEB	2aedbf1d-c8b7-4d5d-83ee-e38872c37d4f	2025-10-30	Warnings	Exact identifier application number: M017
Hydrocortisone	HYDROCORTISONE SPRAY	Meijer Distribution Inc.	28daaf97-b0b3-7a54-e063-6294a90a23f1	2025-10-30	Warnings	Exact identifier application number: M017
Calamine Plus	CALAMINE PLUS PRAMOXINE HCL	Meijer Distribution Inc.	03c46823-0b1f-4101-e063-6294a90aaf94	2025-10-30	Warnings	Exact identifier application number: M017
Extra Strength Itch Relief	DIPHENHYDRAMINE HCL AND ZINC ACETATE	Meijer Distribution Inc	02f9e270-6047-83b6-e063-6394a90afc27	2025-10-30	Warnings	Exact identifier application number: M017
Muscle Rub Pain Reliever Gel	MENTHOL, UNSPECIFIED FORM	Universal Distribution Centre LLC	18536e21-afc3-8447-e063-6394a90aabae	2025-10-30	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