Home NDC 50804-191 Goodsense Oral Pain Relief
Product NDC 50804-191
11-digit product format 508040191
Labeler code 50804
Product ID 50804-191_483a8e8b-e815-3834-e063-6294a90a3225
Type HUMAN OTC DRUG
Nonproprietary name Benzocaine
Dosage form GEL
Route TOPICAL
Labeler Geiss, Destin and Dunn, Inc.
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2014-05-09
Substance BENZOCAINE
Active strength 20 g/100g
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
NDC exclude flag No
Listing certified through 2027-12-31
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 · 18 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 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 50804-191-10 I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 50804-191-10 I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…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 50804-191-10 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 50804-191-10 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 50804-191-10 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 50804-191-10 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 50804-191-10 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 50804-191-10 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 50804-191-10 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 Goodsense Oral Pain Relief
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZOCAINE 20 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination U3RSY48JW5 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 238910 Internal RxNorm 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 50804-191-10 Goodsense Oral Pain Relief 1 in 1 CARTON GEL 1 10 50804-191-10 Goodsense Oral Pain Relief 14 g in 1 TUBE GEL 14 10
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded BENZOCAINE ACTIVE INGREDIENT U3RSY48JW5 GOODSENSE ORAL PAIN RELIEF (BENZOCAINE) GEL [GEISS, DESTIN AND DUNN, INC.] 1 BENZOCAINE ACTIVE MOIETY U3RSY48JW5 GOODSENSE ORAL PAIN RELIEF (BENZOCAINE) GEL [GEISS, DESTIN AND DUNN, INC.] 1 GLYCERIN INACTIVE INGREDIENT PDC6A3C0OX GOODSENSE ORAL PAIN RELIEF (BENZOCAINE) GEL [GEISS, DESTIN AND DUNN, INC.] 1 MINT INACTIVE INGREDIENT FV98Z8GITP GOODSENSE ORAL PAIN RELIEF (BENZOCAINE) GEL [GEISS, DESTIN AND DUNN, INC.] 1 POLYETHYLENE GLYCOL 400 INACTIVE INGREDIENT B697894SGQ GOODSENSE ORAL PAIN RELIEF (BENZOCAINE) GEL [GEISS, DESTIN AND DUNN, INC.] 1 POLYETHYLENE GLYCOL 4000 INACTIVE INGREDIENT 4R4HFI6D95 GOODSENSE ORAL PAIN RELIEF (BENZOCAINE) GEL [GEISS, DESTIN AND DUNN, INC.] 1 SACCHARIN SODIUM INACTIVE INGREDIENT SB8ZUX40TY GOODSENSE ORAL PAIN RELIEF (BENZOCAINE) GEL [GEISS, DESTIN AND DUNN, INC.] 1 SORBITOL INACTIVE INGREDIENT 506T60A25R GOODSENSE ORAL PAIN RELIEF (BENZOCAINE) GEL [GEISS, DESTIN AND DUNN, INC.] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 50804-191 GOODSENSE ORAL PAIN RELIEF (BENZOCAINE) GEL [GEISS, DESTIN AND DUNN, INC.] 9 Current NDC, Legacy NDC, 2 package rows 20220526_eb461b70-d10f-4e11-8374-e43713f3504d.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
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 50804-191-10 50804019110 1 TUBE in 1 CARTON (50804-191-10) / 14 g in 1 TUBE 1 tube 2018-12-18 0000-00-00 No No Current