Home NDC 72127-0803 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.
FDA-Initiated Inactive NDC Indexing# 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 98 of 153 · 3,057 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Carmex Variety Pack Classic Medicated Lip Balm Lip Balm SPF 15 CAMPHOR (SYNTHETIC), WHITE PETROLATUM, OCTINOXATE, OXYBENZONE Carma Laboratories, Inc. 3a36a241-37a9-445a-a6e0-97709a7457a8 2025-03-19 Warnings Exact identifier application number: M017 Herb Analgesic HERB ANALGESIC PASTE Changsha Maocheng Trading Co., Ltd 29373587-9eff-6ea0-e063-6394a90a23b2 2025-03-18 Warnings Exact identifier application number: M017 DEBACHERE Butt Balm After Play Care Multi Symptoms Relief BENZOCAINE, BENZALKONIUM CHLORIDE DE.BACHERE USA LLC f469b446-58a0-4be3-884f-d622b9d074f8 2025-03-17 Warnings Exact identifier application number: M017 Auvon 4% Menthol Pain Relief Gel MENTHOL SHENZHEN YUWEN E-COMMERCE CO., LTD. 2dacd6fe-7d69-bcf0-e063-6294a90a0351 2025-03-14 Warnings Exact identifier application number: M017 Eagle Medicated MENTHOL METHYL SALICYLATE Borden Company (Private) Limited 1ee49cad-84d4-42cf-aa83-c0da6f1b1b84 2025-03-14 Warnings Exact identifier application number: M017 AY BENDITO THERMOACTIVE MENTHOL, CAMPHOR AY BENDITO INTERNATIONAL, INC 304d71b6-91c8-b2b6-e063-6394a90ab669 2025-03-14 Warnings Exact identifier application number: M017 Hot/Cold Medicated Patch HOT COLD PATCH Dynarex 999881b3-287e-d975-e053-2995a90a87e3 2025-03-14 Warnings Exact identifier application number: M017 Capsaicin 0.025% CAPSAICIN 0.025% Marcella Health 3054e7fd-cab2-7f77-e063-6294a90a498d 2025-03-14 Warnings Exact identifier application number: M017 MENTHOL 5% MENTHOL 5% Marcella Health 30914c0a-fbda-5674-e063-6294a90aba5b 2025-03-14 Warnings Exact identifier application number: M017 Peppermint Soothing Patch CAMPHORIC ACID, MENTHOL, UNSPECIFIED FORM Henan Lijitang Medical Technology Co., Ltd. 30361dd4-1f3d-ac5e-e063-6294a90a23bc 2025-03-13 Warnings Exact identifier application number: M017 AVCOO Menthol Pain Relief Patch MENTHOL ADP Health Limited 3036804b-16c3-0c88-e063-6394a90a3084 2025-03-13 Warnings Exact identifier application number: M017 LIDOCAINE 4% LIDOCAINE 4% Marcella Health 303d9462-cbfb-6251-e063-6394a90a7065 2025-03-13 Warnings Exact identifier application number: M017 XeroBurn Burn Gel LIDOCAINE HYDROCHLORIDE Dynarex Corporation 58985046-ca9c-12be-e053-2991aa0abe72 2025-03-13 Warnings Exact identifier application number: M017 Post Treatment Repair Cream HYDROCORTISONE Vege Labs LLC. 302d4327-354b-a252-e063-6394a90a20b6 2025-03-12 Warnings Exact identifier application number: M017 TheraCare Pain Relief 4% Lidocaine LIDOCAINE Veridian Healthcare 2d3fc030-5d53-2acd-e063-6294a90a11ab 2025-03-11 Warnings Exact identifier application number: M017 Cold Hot Medicated Patch 5% Menthol MENTHOL Veridian Healthcare 2d413707-794c-2fa8-e063-6394a90a06bf 2025-03-11 Warnings Exact identifier application number: M017 Cold Hot Medicated Patch 5% Menthol MENTHOL Veridian Healthcare 2d04799f-946d-ac53-e063-6294a90afeb7 2025-03-11 Warnings Exact identifier application number: M017 Muscle and Joint Care LIDOCAINE Vege Labs LLC. 301966b5-b535-dc04-e063-6394a90aec17 2025-03-11 Warnings Exact identifier application number: M017 Arctic Blast Pain Releiving MENTHOL, CAMPHOR (SYNTHETIC) Nutriomo Labs Pte, Ltd d5e7d26d-4f63-4b7b-a173-fe3a794c8459 2025-03-10 Warnings Exact identifier application number: M017 Anti Itch WALGREEN Walgreens 30014ff0-2519-4031-e063-6394a90ae07b 2025-03-10 Warnings Exact identifier application number: M017
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