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.

Identifier, FDA.report destination table
Identifier	FDA.report destination
eb461b70-d10f-4e11-8374-e43713f3504d	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
Effective	Related label
2026-01-12	GoodSense Oral Pain Relief Gel 0.5oz (191)
2025-01-30	GoodSense Oral Pain Relief Gel 0.5oz (191)
2022-02-18	GoodSense Oral Pain Relief Gel 0.5oz (191)
2022-01-28	GoodSense Oral Pain Relief Gel 0.5oz (191)

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 Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
50804-191-10	GM - Gram	50804-191	1d0f7c83-238c-4699-aa38-2c3274e5cf08	1	2019-10-07

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
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 83 of 151 · 3,020 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
SYNC PRO	SYNC RELIEF PRO CREAM	iON Pharma, LLC	3a3e91d6-732b-dca9-e063-6394a90a06d4	2025-07-28	Warnings	Exact identifier application number: M017
Careland Pain Relief	METHYL SALICYLATE, MENTHOL	Planet (Anhui) Pharmaceutical Co., Ltd.	83f36771-1033-4fd0-a0e6-82c1dcfedeee	2025-07-28	Warnings	Exact identifier application number: M017
Rite Aid anti-itch	HYDROCORTISONE	Rite Aid Corporation	2a232dd1-9071-4c55-a7f7-19d8404b99a6	2025-07-28	Warnings	Exact identifier application number: M017
Hydrocortisone Plus 12 Moisturizers	HYDROCORTISONE	RITE AID CORPORATION	05598255-3e7a-46a5-ae7e-dcfcb616d59d	2025-07-28	Warnings	Exact identifier application number: M017
Inked Inspired	LIDOCAINE HCL	Prodigy Media Inc	54fb2860-7e63-4598-953a-170226e613e9	2025-07-28	Warnings	Exact identifier application number: M017
Ujhay Hydrocortisone Ointment.	UJHAY HYDROCORTISONE OINTMENT	Guangdong Quadrant Ecological Technology Co., Ltd.	3af59276-8e6a-0603-e063-6394a90a1f9b	2025-07-27	Warnings	Exact identifier application number: M017
SANA SANA Menthol External Analgesic	MENTHOL	Alquimia Najulam S de RL de CV	8b7edd51-e08a-4e01-9df0-8305ce17b418	2025-07-25	Warnings	Exact identifier application number: M017
Hydrocortisone Intensive Healing Formula	HYDROCORTISONE	TARGET Corporation	682b737f-e453-4079-bf31-47a9485c7897	2025-07-25	Warnings	Exact identifier application number: M017
Chigg Away	BENZOCAINE	Pierson Laboratories, Inc.	8372e7c1-f145-4bc5-85ab-cf831abe70ce	2025-07-24	Warnings	Exact identifier application number: M017
Chigg Away	BENZOCAINE	Pharma Nobis, LLC	e42fa1c6-d804-630f-e053-2995a90add6b	2025-07-24	Warnings	Exact identifier application number: M017
Cannarelief 2000mg	MENTHOL	Earthmed LLC	01f810de-52ba-8beb-e063-6394a90a61c0	2025-07-24	Warnings	Exact identifier application number: M017
CHING WAN HUNG SOOTHING HERBAL BALM	MENTHOL	TIANJIN DARENTANG JINGWANHONG PHARMACEUTICAL CO., LTD.	ffadc904-8e9d-4cb8-815a-d583bbdb3f0b	2025-07-24	Warnings	Exact identifier application number: M017
PT Elite Premium Pain Relief	CAPSAICIN, MENTHOL	PT ELITE PRODUCTS LLC	ad251821-4c58-425d-bdcb-8dd9bd41b713	2025-07-23	Warnings	Exact identifier application number: M017
Whipped Butter SPF 50	ZINC OXIDE	Bloomeffects, Inc	374b62d8-e012-591f-e063-6294a90aef93	2025-07-23	Warnings	Exact identifier application number: M017
Game On Xtreme	MENTHOL, UNSPECIFIED FORM	Natural Essentials Inc.	5a1b6192-d537-42b3-add8-22c63e7c986c	2025-07-23	Warnings	Exact identifier application number: M017
AMRUTANJAN RELIEF PAIN BALM	CAMPHOR , MENTHOL, METHYL SALICYLATE	AMRUTANJAN HEALTH CARE LIMITED	ddee6714-8b18-4d87-944b-8467fda22e6b	2025-07-23	Warnings	Exact identifier application number: M017
Stopain Extra Strength Gel	MENTHOL	Troy Manufacturing, Inc.	8bb89002-d7a2-4bee-b5a5-1fd1949273ef	2025-07-22	Warnings	Exact identifier application number: M017
Hielo Ardiente	MENTHOL	Menper Distributors, Inc.	97ec516c-d2bc-47ce-82fe-bd68445d9570	2025-07-22	Warnings	Exact identifier application number: M017
La Flecha Japonesa	METHYL SALICYLATE	Menper Distributors, Inc.	08819ad0-97c2-49bd-b923-535b94a27167	2025-07-22	Warnings	Exact identifier application number: M017
Veneno de Abeja Aceite De Vibora Brand	METHYL SALICYLATE	Menper Distributors Inc.	ad940dc8-9403-44cf-aed3-6e538cbe488b	2025-07-22	Warnings	Exact identifier application number: M017

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
U3RSY48JW5	BENZOCAINE	94-09-7	BENZOCAINE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
238910	benzocaine 20 % Oral Gel	PSN	eb461b70-d10f-4e11-8374-e43713f3504d	10
238910	benzocaine 0.2 MG/MG Oral Gel	SCD	eb461b70-d10f-4e11-8374-e43713f3504d	10
238910	benzocaine 20 % (180-220 MG per 1 GM) Oral Gel	SY	eb461b70-d10f-4e11-8374-e43713f3504d	10

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

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
GoodSense Oral Pain Relief Gel 0.5oz (191)	Geiss, Destin and Dunn, Inc.	2026-01-12	HUMAN OTC DRUG LABEL	10