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 30 of 153 · 3,057 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join RICHTOFIT RAPID ACTIVE ARTHRITIS MENTHOL AND CAMPHOR RICHTOFIT LIMITED LIABILITY COMPANY 4b1cdab1-3e50-4ec3-e063-6394a90af75e 2026-03-12 Warnings Exact identifier application number: M017 5Kind DMSO 4 Lidocaine HCl Pain Relieving LIDOCAINE HYDROCHLORIDE, MENTHOL 5KIND TRADING LTD 67d8d045-7fa0-46c2-8072-645d8823903b 2026-03-11 Warnings Exact identifier application number: M017 Rapid Relief PAIN RELIEF PATCH LIDOCAINE 4% RAPID AID VIET NAM COMPANY LIMITED 4ca541b4-7afe-77c5-e063-6294a90ad692 2026-03-10 Warnings Exact identifier application number: M017 Lidocaine Cream, 4% LIDOCAINE IPG PHARMACEUTICALS, INC. 7775bfdd-7eac-4f09-b83f-fc4a16a24558 2026-03-10 Warnings Exact identifier application number: M017 MENTHOL, CAMPHOR MENTHOL, CAMPHOR CHEMCO CORPORATION 4c989283-9a27-e8d2-e063-6294a90a8bfa 2026-03-09 Warnings Exact identifier application number: M017 Prequel Anti-Itch Solution Medicated Calming MEDICATED CALMING LOTION The Center Brands, LLC 419fa45b-992b-676e-e063-6394a90add81 2026-03-09 Warnings Exact identifier application number: M017 Careland Lidocaine 4 Plus Menthol Pain Relieving Gel Patches for back, neck shoulders knees and elbows with border LIDOCAINE, MENTHOL Planet (Anhui) Pharmaceutical Co., Ltd. 1fda69f7-2bb6-42fc-bcef-677e7b3d7f01 2026-03-09 Warnings Exact identifier application number: M017 Careland Lidocaine 4 plus menthol pain relieving gel-patches with border for knee MENTHOL, LAUROCAPRAM Planet (Anhui) Pharmaceutical Co., Ltd. 7577625c-87eb-4639-aeab-8a2ab97033fd 2026-03-09 Warnings Exact identifier application number: M017 Careland Lidocaine Pain Relieving LIDOCAINE Planet (Anhui) Pharmaceutical Co., Ltd. 7de99b81-b3b3-49f1-8aa7-2ff42e1b46a4 2026-03-09 Warnings Exact identifier application number: M017 Rapid Relief PAIN RELIEF PATCH LIDOCAINE 4% RAPID AID VIET NAM COMPANY LIMITED 4ca35030-958c-8f62-e063-6294a90a4d63 2026-03-09 Warnings Exact identifier application number: M017 Welmate Lidocaine Pain Relieving Patch LIDOCAINE YYBA Corp cff71b75-fc4e-29ac-e053-2995a90abd50 2026-03-06 Warnings Exact identifier application number: M017 Heal and Rescue Bunion Pain Relief LIDOCAINE HCL, MENTHOL Rooftop Consumer Health, Inc 4c60d4d3-e0a9-6f93-e063-6394a90a16af 2026-03-06 Warnings Exact identifier application number: M017 JUST CBD - PAIN RELIEF MENTHOL, CAMPHOR Just Brands LLC 4c493c0b-c58e-cb56-e063-6394a90a9395 2026-03-05 Warnings Exact identifier application number: M017 Hug a BooBoo Medicated booboo Wipes BENZOCAINE Lights Medical Manufacture Co., Ltd. 509aaafc-2ef7-4205-818c-7ff5b146e159 2026-03-04 Warnings Exact identifier application number: M017 CVS Foot Pain LIDOCAINE HYDROCHLORIDE CVS Pharmacy 4c3350c3-2e3e-093c-e063-6394a90a3475 2026-03-04 Warnings Exact identifier application number: M017 Game On Sport MENTHOL Natural Essentials, Inc 4c3411dc-5378-bd93-e063-6394a90a8406 2026-03-04 Warnings Exact identifier application number: M017 Hydrocortisone 1% HYDROCORTISONE Trifecta Pharmaceuticals Usa Llc f4d4a56b-b4b7-9a07-e053-2a95a90ad853 2026-03-04 Warnings Exact identifier application number: M017 Hydrocortisone 1% HYDROCORTISONE Trifecta Pharmaceuticals Usa Llc 9987165c-1a0f-dd57-e053-2a95a90ae735 2026-03-04 Warnings Exact identifier application number: M017 Walgreens Unscented Pain Relieving LIDOCAINE HYDROCHLORIDE, BENZYL ALCOHOL Walgreen Co. 41eadb4f-2ca5-42a1-e063-6294a90ab4e2 2026-03-04 Warnings Exact identifier application number: M017 Careland Pain Relief Patch Plus LIDOCAINE Planet (Anhui) Pharmaceutical Co., Ltd. d55d8a9e-ed2b-4c9b-9ecb-6ec1fd43c9e3 2026-03-04 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