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 82 of 152 · 3,029 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Aruba Aloe Alcoholada LIDOCAINE HYDROCHLORIDE Aruba Aloe Balm NV f56c62b0-75db-4499-858e-54e10b0e140a 2025-08-07 Warnings Exact identifier application number: M017 SurviveX Hydrocortisone Cream HYDROCORTISONE Nantong Health & Beyond Hygienic Products Inc. 3bd1da8d-5142-798c-e063-6294a90a7be6 2025-08-07 Warnings Exact identifier application number: M017 Arthcal SOOTHING PAIN RELIEF MASSAGE SOOTHING PAIN RELIEF MASSAGE Beijing JUNGE Technology Co., Ltd. 3524ad62-0ed6-f2e5-e063-6394a90a3283 2025-08-06 Warnings Exact identifier application number: M017 Alumier MD Intensive Recovery HYDROCORTISONE Alumier Labs d9b79ea1-6558-543c-e053-2995a90ae53e 2025-08-06 Warnings Exact identifier application number: M017 Good Neighbor Roll-on Pain Relief LIDOCAINE HCL Amerisource Bergen a0c3adbf-fa35-47c0-9db3-459ce9a106ac 2025-08-06 Warnings Exact identifier application number: M017 Good Neighbor Roll-on Menthol Pain Relief Gel MENTHOL Amerisource Bergen bd557323-0003-4ee6-b22d-a72d621c7de4 2025-08-05 Warnings Exact identifier application number: M017 Earthmed FS Pain relieving balm MENTHOL Earthmed LLC 3ba4e769-fec6-52d9-e063-6394a90a65d4 2025-08-05 Warnings Exact identifier application number: M017 HYDROCORTISONE HYDROCORTISONE HF Acquisition Co LLC, DBA HealthFirst 3ba6a5ec-fda2-b2a6-e063-6294a90ac9b6 2025-08-05 Warnings Exact identifier application number: M017 Kocowo Lidocaine Pain Relief Gel-Patch LIDOCAINE PAIN RELIEF GEL-PATCH Henan Enokon Medical Instrument Co., Ltd. 3b82989d-7cc3-23d3-e063-6294a90ae2a3 2025-08-03 Warnings Exact identifier application number: M017 Menthol pain relief patches MENTHOL Menthol pain relief patch 3b5fd718-3f86-f7a7-e063-6294a90a8c52 2025-08-02 Warnings Exact identifier application number: M017 Graphene Far Infrared Herbal Pain Relief Patches CORYDALIS RHIZOME Changsha Maocheng Trading Co., Ltd 3b604a3c-fe91-7096-e063-6394a90afe04 2025-08-02 Warnings Exact identifier application number: M017 Active Recovery Pain Relief CAMPHOR, MENTHOL Charlotte's Web, Inc. 3a9f9ca0-3d8a-796a-e063-6394a90a790c 2025-08-01 Warnings Exact identifier application number: M017 Active Recovery Pain Relief Stick CAMPHOR, MENTHOL Charlottes Web, Inc. 3aa037c6-6109-b52e-e063-6394a90a215b 2025-08-01 Warnings Exact identifier application number: M017 PM Recovery Pain Relief CAMPHOR, MENTHOL Charlotte's Web, Inc. 3aa08859-809d-de8c-e063-6394a90a8e25 2025-08-01 Warnings Exact identifier application number: M017 Wish ultra winter ice MENTHOL LJ Pharma b4c5487c-1314-4d63-96df-077e72e7ee95 2025-08-01 Warnings Exact identifier application number: M017 Rugged Fit Pain Relief Roll On MENTHOL, METHYL SALICYLATE SYSTEM4BOOK LLC 39d68734-981c-14d7-e063-6294a90a4919 2025-08-01 Warnings Exact identifier application number: M017 ICY FREEZE MENTHOL, UNSPECIFIED FORM Natural Essentials, Inc. 28fdb049-b297-4358-9447-7d69ba879702 2025-08-01 Warnings Exact identifier application number: M017 Cortizone 10 Cooling HYDROCORTISONE Chattem, Inc. 14d9fce2-9f54-4204-83cb-161de8a303f0 2025-08-01 Warnings Exact identifier application number: M017 Bravado Labs Numbing LIDOCAINE HCL Prodigy Media Inc 8c43f5b5-b911-4a7a-b2d1-56a09c54b001 2025-07-30 Warnings Exact identifier application number: M017 Chimera GUARD LIDOCAINE PAIN RELIEFING PATCH Hangzhou Rongna Health Technology Co., Ltd. 3721c984-1993-6265-e063-6394a90af23f 2025-07-29 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