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 24 of 153 · 3,057 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
A Health Itch Relief Gel	ITCH RELIEF GEL	Pharma Nobis, LLC	4f80c403-c760-31ec-e063-6394a90a61c9	2026-04-15	Warnings	Exact identifier application number: M017
Family Care Antibiotic Pain Relief 0.33oz	ANTIBIOTIC PAIN RELIEF	United Exchange Corp	4f8405fc-3e38-05d9-e063-6394a90a4cda	2026-04-15	Warnings	Exact identifier application number: M017
BiteMD	INSECT BITE RELIEF	Wisconsin Pharmacal Company	4f860c1e-a638-4923-e063-6294a90ae7e2	2026-04-15	Warnings	Exact identifier application number: M017
LavaDerm AfterSun	MENTHOL	Young Living Essential Oils, LC.	4fcddcf1-36db-2f1a-e054-00144ff8d46c	2026-04-15	Warnings	Exact identifier application number: M017
Arlun Numbing Cream	NUMBING CREAM	Guangzhou Jingliang Cosmetics Co., Ltd.	4f8b60f9-03e3-e731-e063-6294a90a3b0a	2026-04-15	Warnings	Exact identifier application number: M017
tuiwaro Numbing Cream	NUMBING CREAM	Guangzhou Jingliang Cosmetics Co., Ltd.	4f66178c-95d9-8c6a-e063-6294a90a2c09	2026-04-14	Warnings	Exact identifier application number: M017
Lidocaine Pain Relief Roll-On	LIDOCAINE 4%	Pharma Nobis, LLC	4f6d9a51-c42e-ca88-e063-6394a90a8659	2026-04-14	Warnings	Exact identifier application number: M017
Hot/Cold Menthol 16% Roll-On	HOT/COLD MENTHOL 16% ROLL-ON	Pharma Nobis, LLC	4f6f5a0b-3bfa-289e-e063-6294a90a94b3	2026-04-14	Warnings	Exact identifier application number: M017
Sting Relief Swab	BENZOCAINE	4 Visions LLC	4f76a8c5-fde6-eee0-e063-6394a90a09f8	2026-04-14	Warnings	Exact identifier application number: M017
Signature Pain Relief Cream	4% LIDOCAINE	Shengnan (Guangzhou) Cosmetics Co., LTD	4f555b8f-5193-e685-e063-6294a90a7ba2	2026-04-13	Warnings	Exact identifier application number: M017
Deep Numbing Cream	MENTHOL	YITONGBADA (SHENZHEN) INTERNATIONAL TRADE CO., LTD	7943559b-de10-4214-96dc-f9cbac828f46	2026-04-13	Warnings	Exact identifier application number: M017
Hydrocortisone Cream 1%	HYDROCORTISONE CREAM 1% WITH ALOE	Publix Super Markets Inc.	3c45a654-7fec-55b3-e063-6294a90a184b	2026-04-13	Warnings	Exact identifier application number: M017
Hydrocortisone with Aloe	HYDROCORTISONE CREAM 1%	AMERISOURCE BERGEN	4f5aea1c-ae51-4e1a-e063-6294a90a6aa1	2026-04-13	Warnings	Exact identifier application number: M017
ActivICE	MENTHOL	Medline Industries, LP	8465b443-abe9-78fb-e053-2a91aa0ac1d8	2026-04-13	Warnings	Exact identifier application number: M017
4Jointz	MENTHOL	ARP(USA) Pty Ltd	94a5b5f5-abf7-40b3-9dd7-43e2c22f138e	2026-04-13	Warnings	Exact identifier application number: M017
Sumifun Pain Relief Creams	METHYL SALICLATE CAPSAICIN CAMPHOR	Guchutang Biotechnology (Longyan) Co., Ltd	4f3dd96a-d843-d810-e063-6394a90a188e	2026-04-12	Warnings	Exact identifier application number: M017
BonicaEaseX 24 Hour Menthol Pain Relieving	MENTHOL, UNSPECIFIED FORM	Planet (Anhui) Pharmaceutical Co., Ltd.	17fc0cd1-710d-45e6-9513-d7100e3adb42	2026-04-10	Warnings	Exact identifier application number: M017
BonicaEaseX Colorless Roll-On Menthol Pain Relieving	MENTHOL, UNSPECIFIED FORM	Planet (Anhui) Pharmaceutical Co.,Ltd	acf460b4-1b41-4b30-a74a-6c3613119d8e	2026-04-10	Warnings	Exact identifier application number: M017
BonicaEaseX Menthol Pain Relieving	MENTHOL, UNSPECIFIED FORM	Planet (Anhui) Pharmaceutical Co.,Ltd	4d84b4fb-8f55-4b2b-b261-858edb7f3144	2026-04-10	Warnings	Exact identifier application number: M017
HealthWise Pain Relief Gel Patch	CAPSAICIN, MENTHOL	Veridian Healthcare	f5484151-b6da-4f64-867f-87160a4ec2d6	2026-04-10	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