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 53 of 152 · 3,029 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Resinol	PETROLATUM AND RESORCINOL	ResiCal, Inc.	03f57a4a-f94b-4ba6-b709-41cfb6e16261	2025-12-17	Warnings	Exact identifier application number: M017
HealthWise Maximum Pain Relief	LIDOCAINE	Veridian Healthcare	afc3c16d-0076-44b2-ae7e-5f36d4d8088e	2025-12-17	Warnings	Exact identifier application number: M017
HealthWise Max Lidocaine plus Menthol	LIDOCAINE, MENTHOL	Veridian Healthcare	f39a27da-6799-4fc6-97ca-101eac4a9360	2025-12-17	Warnings	Exact identifier application number: M017
HealthWise Original Menthol	MENTHOL	Veridian Healthcare	e4bfb6b0-545e-4fbc-8538-4f41a6be1025	2025-12-17	Warnings	Exact identifier application number: M017
Welly Polka First Aid Kit	HYDROCORTISONE, BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE	Dongguan Shenglian Tins Products Co., Ltd.	d7c4314c-c4c6-4adf-b384-3ac7a7108319	2025-12-17	Warnings	Exact identifier application number: M017
Frankincense and Myrrh Arthritis Pain Therapy	MENTHOL	Wise Consumer Products	2410a199-f4a3-da6c-e063-6394a90aaace	2025-12-17	Warnings	Exact identifier application number: M017
Lidocaine	LIDOCAINE, MENTHOL	Vive Health LLC	462d3b24-643e-91da-e063-6394a90a0e1d	2025-12-17	Warnings	Exact identifier application number: M017
Teevodar Pain Relieving	MENTHOL	Sod-e Biotech Ltd	205b0fef-4f00-db2e-e063-6294a90a93b8	2025-12-17	Warnings	Exact identifier application number: M017
Frankincense and Myrrh Arthritis Pain Relief	MENTHOL	WISE CONSUMER PRODUCTS CO.	116045df-891b-f370-e063-6294a90abe42	2025-12-17	Warnings	Exact identifier application number: M017
Frankincense and Myrrh Intensive Foot Therapy	MENTHOL	Wise Consumer Products	23e56c6b-0f2b-721f-e063-6394a90a1ed0	2025-12-17	Warnings	Exact identifier application number: M017
Tiger Balm Ultra Strength	CAMPHOR (SYNTHETIC) AND MENTHOL	Haw Par Healthcare Ltd.	f0561804-e0f7-495d-9768-9b86a208c51e	2025-12-17	Warnings	Exact identifier application number: M017
Kwan Loong	METHYL SALICYLATE AND MENTHOL	Haw Par Healthcare Ltd.	54bcb26e-786a-403e-9330-11ae9e3c013a	2025-12-17	Warnings	Exact identifier application number: M017
Magsoothium Body Cooling Formula	MENTHOL	Ubu/Elements, Inc.	f7fb6ac9-a920-a440-e053-6394a90aaa35	2025-12-16	Warnings	Exact identifier application number: M017
Magsoothium CBD Body Lavender	MENTHOL	Ubu/Elements, Inc.	f9b87fbe-b889-67a1-e053-6394a90acbcd	2025-12-16	Warnings	Exact identifier application number: M017
Aquaphor Itch Relief	HYDROCORTISONE	Beiersdorf Inc	b1d0333f-ba60-35d8-e053-2995a90af932	2025-12-16	Warnings	Exact identifier application number: M017
Magsoothium CBD Body	MENTHOL	Ubu/Elements, Inc.	00b2ef34-42d7-523c-e063-6294a90a753d	2025-12-16	Warnings	Exact identifier application number: M017
GENTLECARE HAND AND SKIN SANITIZER	BENZALKONIUM CHLORIDE	PARAGON SOLUTIONS US, INC.	16650277-fa62-485e-9a82-7763d2b50168	2025-12-16	Warnings	Exact identifier application number: M017
Welly First Aid Kit Refill	HYDROCORTISONE, BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, LIDOCAINE	Dongguan Shenglian Tins Products Co., Ltd.	4bc93855-4009-4b49-9fb4-e5864054153d	2025-12-16	Warnings	Exact identifier application number: M017
LidocainePain pain reliving gel-patch	PAIN RELIVING GEL-PATCH	Shenzhen Yuetai Electronic Commerce Co., Ltd	461ebbdd-0f26-a333-e063-6394a90a7a3e	2025-12-16	Warnings	Exact identifier application number: M017
Zestama	CAPSAICIN	V2 Pharma LLC	c9b46759-b8df-4ff4-815e-8e032c2635c0	2025-12-15	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