GoodSense Medicated Dandruff

Product NDC: 50804-883
11-digit product format: 508040883
Labeler code: 50804
Product ID: 50804-883_f5356ff2-25b0-42ab-92de-0cdf350de88d
Type: HUMAN OTC DRUG
Nonproprietary name: Selenium Sulfide
Dosage form: SHAMPOO
Route: TOPICAL
Labeler: GOODSENSE
Application: M032
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2018-03-01
Substance: SELENIUM SULFIDE
Active strength: 10 mg/mL
NDC exclude flag: No
Listing certified through: 2026-12-31
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 · 34 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Snapshot	Source SHA-256
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	50804-883-01	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	50804-883-01	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	50804-883-01	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	50804-883-01	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	50804-883-01	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	50804-883-01	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	50804-883-01	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	50804-883-01	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded product	product		`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	50804-883-01	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded product	product		`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	50804-883-01	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded product	product		`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	50804-883-01	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded product	product		`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded package	package	50804-883-01	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded product	product		`834df4deac94…`	`adcc014656a3…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded package	package	50804-883-01	`834df4deac94…`	`adcc014656a3…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded product	product		`1332a3947898…`	`d4bfe170f9cd…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded package	package	50804-883-01	`1332a3947898…`	`d4bfe170f9cd…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded product	product		`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded package	package	50804-883-01	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded product	product		`86f5da6cb304…`	`a595104c45d7…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	50804-883-01	`86f5da6cb304…`	`a595104c45d7…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded product	product		`bd6a592717d7…`	`303034d00443…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	50804-883-01	`bd6a592717d7…`	`303034d00443…`

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 Medicated Dandruff
Brand name suffix: Anti-Seborrheic Dermatitis, Anti-Dandruff
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
SELENIUM SULFIDE	10 mg/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
Z69D9E381Q	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
204642	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
21291e29-57ab-4761-8e8c-eef43ca65b24	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
362d7abb-94e6-4c60-9a58-266894157713	Product name	1	20231023
6bd95106-a412-1dad-b9cc-4cb74bfb27ce	Product name	2	20230315
f1e0dc7e-7d61-4625-b6d9-4894927679d7	Product name	2	20211025
e4870509-7e28-6f92-f0be-dd3dd889a9cf	Product name	5	20200810
6e9d4a47-c464-b93e-aebc-ad7bffc9c4cd	Product name	2	20190619
444b3e50-f226-46ef-bfca-2e7035d140cd	Product name	1	20190611
816b97af-edc5-4060-aff1-b814bdbcad50	Product name	1	20190415
7cda52fc-125f-421c-8fea-bc1974370c49	Product name	2	20180703
419aab54-5d5a-4146-9453-026d4a9991be	Product name	2	20170525
d5e51f11-ad28-caa4-4b49-4143974782ad	Product name	1	20150831
290f523a-f9db-9774-b5a9-e1f908ac1782	Product name	1	20150828
89dac932-b90a-4410-9ab1-84c53e57de25	Product name	1	20150316
5668b646-cd56-c3c7-bdea-3f6b1a8840db	Product name	1	20140508
684ea482-2e8b-14af-5664-b98f1e402036	Product name	1	20140508
810ab97e-f109-f41c-7c83-6a652a9cbf43	Product name	1	20140508
87711080-88eb-65c5-b2dd-bf99e700a372	Product name	1	20140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2dd	Product name	1	20140508
b060cc1a-fe47-856b-0b77-4448b5963de8	Product name	1	20140508
c6b65c52-69c7-df49-550a-a50c137f6218	Product name	1	20140508
ec2149b3-5c6d-5344-f757-c86411073075	Product name	1	20140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
50804-883-01	2025-12-04	C162847	48780-1	d6a99b39-5b33-a426-e053-dadaa90af4c2	GoodSense ® Medicated Dandruff Shampoo Anti-Seborrheic Dermatitis, Anti-Dandruff
50804-883-01	2022-01-28	C162847	48780-1	d6a99b39-5b33-a426-e053-dadaa90af4c2	GoodSense ® Medicated Dandruff Shampoo Anti-Seborrheic Dermatitis, Anti-Dandruff

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
50804-883-01	GoodSense Medicated DandruffAnti-Seborrheic Dermatitis, Anti-Dandruff	325 mL in 1 BOTTLE, PLASTIC	SHAMPOO	325		3

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
50804-883-01	ML - Milliliter	50804-883	a70737a8-234b-4be6-b353-d7dd27da9deb	1	2024-03-12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
50804-883	GOODSENSE MEDICATED DANDRUFF ANTI-SEBORRHEIC DERMATITIS, ANTI-DANDRUFF (SELENIUM SULFIDE) SHAMPOO [GEISS, DESTIN & DUNN, INC.]	2	Current NDC, Legacy NDC, 1 package rows	20200701_21291e29-57ab-4761-8e8c-eef43ca65b24.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 11 of 31 · 615 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Everyday Clean Dandruff	PYRITHIONE ZINC	Retail Business Services, LLC	8fb44204-b763-4aa5-a6db-94d1b4d98b65	2026-02-06	Warnings, Adverse reactions	Exact identifier application number: M032
Dandruff	PYRITHIONE ZINC	Retail Business Services, LLC	c1d8c237-1ca8-4fdb-ba94-787d3a9e6111	2026-02-06	Warnings, Adverse reactions	Exact identifier application number: M032
Dry Scalp Dandruff	PYRITHIONE ZINC	Retail Business Services, LLC	592ec7c5-44b8-405b-88a2-f02aa6c620f0	2026-02-06	Warnings, Adverse reactions	Exact identifier application number: M032
Dry Scalp Care	PYRITHIONE ZINC	Retail Business Services, LLC	37357176-913d-4dd7-a565-ad21d4ad60a8	2026-02-06	Warnings, Adverse reactions	Exact identifier application number: M032
Dandruff	PYRITHIONE ZINC	Retail Business Services, LLC	c8c82495-f09a-4ec1-9036-e464845e02f9	2026-02-06	Warnings, Adverse reactions	Exact identifier application number: M032
2 in 1 Dandruff	PYRITHIONE ZINC	Retail Business Services, LLC	ec9d36ae-cf4e-4841-a13e-5cb0fe64c4fa	2026-02-06	Warnings, Adverse reactions	Exact identifier application number: M032
2 in 1 Dandruff	PYRITHIONE ZINC	Retail Business Services, LLC	841429c3-e15c-41cc-9ca8-6b5a21a21587	2026-02-06	Warnings, Adverse reactions	Exact identifier application number: M032
Dandruff	PYRITHIONE ZINC	Publix Super Markets, Inc.	56c2b8c2-69ea-4343-ae69-43f5966261c2	2026-02-05	Warnings, Adverse reactions	Exact identifier application number: M032
Dandruff	PYRITHIONE ZINC	Publix Super Markets, Inc.	8a204a2c-6dcb-4fc4-b265-9b95da204236	2026-02-05	Warnings, Adverse reactions	Exact identifier application number: M032
Everyday Clean Dandruff	PYRITHIONE ZINC	Harris Teeter	8594a944-a67e-4dbe-8d31-7099410ff484	2026-02-04	Warnings, Adverse reactions	Exact identifier application number: M032
Everyday Clean Dandruff	PYRITHIONE ZINC	Amazon.Com Services LLC	e30896df-e4b2-4b1f-a226-a26055a4a121	2026-02-03	Warnings, Adverse reactions	Exact identifier application number: M032
Oribe Serene Scalp Anti Dandruff	ORIBE SERENE SCALP ANTI DANDRUFF	Oribe Hair Care LLC	34c4abb5-6f96-4866-a37f-4f9be6c43f2b	2026-01-30	Warnings	Exact identifier application number: M032
NATUREPLEX PSORIASIS	SALICYLIC ACID	Natureplex, LLC	1efa3e8d-f80b-44f4-a233-187e3329dd8f	2026-01-29	Warnings	Exact identifier application number: M032
Head and Shoulders Charcoal Daily	PYRITHIONE ZINC	The Procter & Gamble Manufacturing Company	69abc8fa-eee5-d36f-e053-2991aa0a940b	2026-01-28	Warnings	Exact identifier application number: M032
WeCare Anti-Dandruff	ANTIDANDRUFF SHAMPOO	Dynarex Corporation	7fad58a3-5537-f87a-e053-2991aa0a7cdb	2026-01-28	Warnings	Exact identifier application number: M032
TriDerma Psoriasis Control Face and Body Cream	SALICYLIC ACID	Genuine Virgin Aloe Corporation	66eeaf72-1fb4-4df0-9198-41f1143c67b3	2026-01-27	Warnings	Exact identifier application number: M032
TRIDERMA Psoriasis Control	SALICYLIC ACID	Genuine Virgin Aloe Corporation	16ba7145-0e8c-48b8-b557-43ac1be317ac	2026-01-27	Warnings	Exact identifier application number: M032
DHS tar gel	COAL TAR	Person and Covey	e17bd664-748b-417c-a247-9acc7bc7eec3	2026-01-23	Warnings	Exact identifier application number: M032
Therapeutic TPlus Salicylic Acid Anti-dandruff, anti-seborrheic dermatitis, anti-psoriasis	SALICYLIC ACID	Garcoa, Inc.	620617e3-0ee1-469a-ad2b-0dda957627cc	2026-01-21	Warnings	Exact identifier application number: M032
Aloe Coal 02 Conditioner	PYRITHIONE ZINC	T. SPRUILL, LLC	e8e1fbe8-7de3-4a8e-bace-b7b2e4db1828	2026-01-19	Warnings	Exact identifier application number: M032

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
Z69D9E381Q	SELENIUM SULFIDE	7488-56-4	SELENIUM SULFIDE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
204642	selenium sulfide 1 % Medicated Shampoo	PSN	21291e29-57ab-4761-8e8c-eef43ca65b24	3
204642	selenium sulfide 10 MG/ML Medicated Shampoo	SCD	21291e29-57ab-4761-8e8c-eef43ca65b24	3
204642	selenium sulfide 1 % Lotion Shampoo	SY	21291e29-57ab-4761-8e8c-eef43ca65b24	3
204642	selenium sulfide 1 % Medicated Shampoo	SY	21291e29-57ab-4761-8e8c-eef43ca65b24	3

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
50804-883-01	50804088301	325 mL in 1 BOTTLE, PLASTIC (50804-883-01)	325 ml	2018-03-01	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
GoodSense Medicated Dandruff Anti-Seborrheic Dermatitis, Anti-Dandruff	GOODSENSE \| Garcoa, Inc.	2020-06-30	HUMAN OTC DRUG LABEL	3