Good Sense Nasal

Product NDC: 0113-0304
11-digit product format: 001130304
Labeler code: 0113
Product ID: 0113-0304_140a1a6e-2f5d-453b-b593-cd00fe83c1d2
Type: HUMAN OTC DRUG
Nonproprietary name: oxymetazoline hydrochloride
Dosage form: SPRAY
Route: NASAL
Labeler: L. Perrigo Company
Application: M012
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 1989-09-15
Substance: OXYMETAZOLINE HYDROCHLORIDE
Active strength: .5 mg/mL
Pharmacologic classes: Imidazolines [CS], Increased Sympathetic Activity [PE], Vasoconstriction [PE], Vasoconstrictor [EPC]
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	0113-0304	0113-0304-72	D	Discontinued by firm		2026-08-10

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 · 11 matching rows.

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

Captured / source date, Snapshot, Source SHA-256 table
Captured / source date	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	`367a005e9d99…`	`383a685ebd0f…`

Additional Listing Data#

Finished product: Yes
Brand name base: Good Sense Nasal
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
OXYMETAZOLINE HYDROCHLORIDE	.5 mg/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
K89MJ0S5VY	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
1000990	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
276d7d3c-c4a7-4754-8845-c38f85aac5f7	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
e67be450-f8e4-4bc1-88bd-1259d379f55f	Product name	1	20210127
c53f3286-4062-4cf5-8355-399519c639a6	Product name	1	20170424
a993dfc5-f219-4460-bde6-30dd724d9ef0	Product name	1	20160818
9869efd7-d6dd-0665-5b67-53adbe6ef15e	Product name	1	20140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
0113-0304-10	Good Sense Nasal	1 in 1 CARTON	SPRAY	1	9
0113-0304-10	Good Sense Nasal	30 mL in 1 BOTTLE, SPRAY	SPRAY	30	9
0113-0304-72	Good Sense Nasal	37 mL in 1 BOTTLE, SPRAY	SPRAY	37	9
0113-0304-72	Good Sense Nasal	1 in 1 CARTON	SPRAY	1	9

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0113-0304-10	ML - Milliliter	0113-0304	f827fba0-4894-429a-92d3-b24b42fd8aab	1	2012-07-24
0113-0304-72	ML - Milliliter	0113-0304	29a9f677-8f87-44c7-8c96-531d5824765e	1	2024-02-14

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
OXYMETAZOLINE HYDROCHLORIDE	ACTIVE INGREDIENT	K89MJ0S5VY	GOOD SENSE NASAL (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [L. PERRIGO COMPANY]	5
OXYMETAZOLINE	ACTIVE MOIETY	8VLN5B44ZY	GOOD SENSE NASAL (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [L. PERRIGO COMPANY]	5
BENZALKONIUM CHLORIDE	INACTIVE INGREDIENT	F5UM2KM3W7	GOOD SENSE NASAL (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [L. PERRIGO COMPANY]	5
BENZYL ALCOHOL	INACTIVE INGREDIENT	LKG8494WBH	GOOD SENSE NASAL (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [L. PERRIGO COMPANY]	5
EDETATE DISODIUM	INACTIVE INGREDIENT	7FLD91C86K	GOOD SENSE NASAL (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [L. PERRIGO COMPANY]	5
POLYETHYLENE GLYCOLS	INACTIVE INGREDIENT	3WJQ0SDW1A	GOOD SENSE NASAL (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [L. PERRIGO COMPANY]	5
POVIDONES	INACTIVE INGREDIENT	FZ989GH94E	GOOD SENSE NASAL (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [L. PERRIGO COMPANY]	5
PROPYLENE GLYCOL	INACTIVE INGREDIENT	6DC9Q167V3	GOOD SENSE NASAL (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [L. PERRIGO COMPANY]	5
SODIUM PHOSPHATE, DIBASIC	INACTIVE INGREDIENT	GR686LBA74	GOOD SENSE NASAL (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [L. PERRIGO COMPANY]	5
SODIUM PHOSPHATE, MONOBASIC	INACTIVE INGREDIENT	3980JIH2SW	GOOD SENSE NASAL (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [L. PERRIGO COMPANY]	5
WATER	INACTIVE INGREDIENT	059QF0KO0R	GOOD SENSE NASAL (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [L. PERRIGO COMPANY]	5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0113-0304	GOOD SENSE NASAL (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [L. PERRIGO COMPANY]	9	Current NDC, Legacy NDC, 4 package rows	20240912_276d7d3c-c4a7-4754-8845-c38f85aac5f7.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 1 of 195 · 3,890 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Daytime Nighttime Intense Flu Relief	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE	Walgreen Company	03aa43fd-4962-4c2c-9edd-e422a629a0e3	2026-08-06	Warnings	Exact identifier application number: M012
Allergy Multi-Symptom	ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE AND PHENYLEPHRINE HCL	ARMY AND AIR FORCE EXCHANGE SERVICE	f311b56f-b959-4070-9b23-82c642dd98b8	2026-08-06	Warnings	Exact identifier application number: M012
Cold Relief Multi-Symptom	ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL	L.N.K. International, Inc.	2ed25f69-89ef-4c50-946a-7e7b9df1ca8a	2026-08-06	Warnings	Exact identifier application number: M012
Eucamint	MENTHOL, CAMPHOR	Indiana Botanic Gardens	d79bc8de-9efb-4996-a55c-accda0f8edb2	2026-08-06	Warnings	Exact identifier application number: M012
DRX CHOICE Daytime and Nighttime Cold and Flu Relief	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL, AND ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE	Raritan Pharmaceuticals Inc	b745f45d-2042-4daa-9932-241836d7734b	2026-08-06	Warnings	Exact identifier application number: M012
Acetaminophen, Dextromethorphan HBr	ACETAMINOPHEN, DEXTROMETHORPHAN HBR	NUVICARE LLC	6713fdff-0e4e-4a9d-b218-34f786339c57	2026-08-06	Warnings	Exact identifier application number: M012
Daytime Cold, Nighttime Cold multi-symptom	ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL	United Natural Foods, Inc. dba UNFI	3b462a5d-d48b-4b73-b5d4-d7944730bbdd	2026-08-06	Warnings	Exact identifier application number: M012
Sinufrin Quick Relief Decongestant	SINUFRIN	Neilmed pharmaceuticals Inc.	0c36a34e-462d-713c-e063-6294a90a1776	2026-08-05	Warnings	Exact identifier application number: M012
No Drip	OXYMETAZOLINE HYDROCHLORIDE	NeilMed Pharmaceuticals Inc	e9b799ad-9164-7f30-e053-2a95a90a00c5	2026-08-05	Warnings	Exact identifier application number: M012
DM Max	DEXTROMETHORPHAN HBR, GUAIFENESIN	Walgreen Company	78edeb7a-4712-4f04-9d76-d5b2d20ce76d	2026-08-04	Warnings	Exact identifier application number: M012
CareOne Nighttime Cold and Flu	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE	American Sales Company	c9342ad2-84dc-4f4c-9b05-c6e5c1c7989e	2026-08-04	Warnings	Exact identifier application number: M012
dg health cold and flu relief	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE	Dolgencorp Inc	3d8ce88e-9f40-4b58-a811-160ddbfb8112	2026-08-04	Warnings	Exact identifier application number: M012
ValuRx Dye Free Allergy Relief	DIPHENHYDRAMINE HCL 25 MG	Shield Pharmaceuticals Corp	ca60a413-b02e-48ce-985d-4d415780c679	2026-08-04	Warnings	Exact identifier application number: M012
Allergy Relief	DIPHENHYDRAMINE HCL	Wal-Mart Stores Inc	150b68ba-3ed4-4533-9118-74e76eaf6e48	2026-08-04	Warnings	Exact identifier application number: M012
Allergy Relief	DIPHENHYDRAMINE HCL	Rite Aid Corporation	ce393bff-498b-42e6-a41c-bbfbc58fb42c	2026-08-04	Warnings	Exact identifier application number: M012
Sinus and Headache	ACETAMINOPHEN AND PHENYLEPHRINE HCL	Cardinal Health 110, LLC. DBA Leader	3b8662bf-3abb-4e54-af9c-5fa1d2e19003	2026-08-04	Warnings	Exact identifier application number: M012
Mucus Relief PE	GUAIFENESIN, PHENYLEPHRINE HCL	Walgreen Company	cb1c1922-5dc6-520d-e77e-e951726d9701	2026-08-04	Warnings	Exact identifier application number: M012
Chest Congestion Relief DM	DEXTROMETHORPHAN HBR, GUAIFENESIN	DOLGENCORP, LLC	da053bc3-e790-4ae9-a406-2629640e97e7	2026-08-04	Warnings	Exact identifier application number: M012
Cold and Flu plus Congestion Nighttime	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HCL	WALMART INC.	1236b463-0073-44b5-a516-5b7c06a40887	2026-08-04	Warnings	Exact identifier application number: M012
daytime nitetime cold and flu	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HCL	Meijer Distribution Inc	80aae1c3-a616-442b-842e-177db957a69c	2026-08-04	Warnings	Exact identifier application number: M012

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
K89MJ0S5VY	OXYMETAZOLINE HYDROCHLORIDE	2315-02-8	OXYMETAZOLINE HYDROCHLORIDE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1000990	oxymetazoline HCl 0.05 % Nasal Spray	PSN	276d7d3c-c4a7-4754-8845-c38f85aac5f7	9
1000990	oxymetazoline hydrochloride 0.5 MG/ML Nasal Spray	SCD	276d7d3c-c4a7-4754-8845-c38f85aac5f7	9
1000990	oxymetazoline hydrochloride 0.05 % Nasal Spray	SY	276d7d3c-c4a7-4754-8845-c38f85aac5f7	9
1000990	oxymetazoline HCl 0.05 % Nasal Spray	PSN	b6fbc0ba-7e88-4ab9-b0fa-1e1e8f9132fe	1
1000990	oxymetazoline HCl 0.05 % Nasal Spray	PSN	f91b7c1f-e074-4767-b9c8-dbf1937a6a0f	1
1000990	oxymetazoline hydrochloride 0.5 MG/ML Nasal Spray	SCD	b6fbc0ba-7e88-4ab9-b0fa-1e1e8f9132fe	1
1000990	oxymetazoline hydrochloride 0.5 MG/ML Nasal Spray	SCD	f91b7c1f-e074-4767-b9c8-dbf1937a6a0f	1
1000990	oxymetazoline hydrochloride 0.05 % Nasal Spray	SY	b6fbc0ba-7e88-4ab9-b0fa-1e1e8f9132fe	1
1000990	oxymetazoline hydrochloride 0.05 % Nasal Spray	SY	f91b7c1f-e074-4767-b9c8-dbf1937a6a0f	1

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
0113-0304-10	00113030410	1 BOTTLE, SPRAY in 1 CARTON (0113-0304-10) / 30 mL in 1 BOTTLE, SPRAY	1989-09-15	0000-00-00	No	No	Current
0113-0304-72	00113030472	1 BOTTLE, SPRAY in 1 CARTON (0113-0304-72) > 37 mL in 1 BOTTLE, SPRAY	1989-09-15	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Perrigo Nasal Spray Drug Facts	Sportpharm LLC	2026-02-06	HUMAN OTC DRUG LABEL	1
Perrigo Nasal Spray Drug Facts	A-S Medication Solutions	2024-10-31	HUMAN OTC DRUG LABEL	1
Perrigo Nasal Spray Drug Facts	L. Perrigo Company	2024-09-08	HUMAN OTC DRUG LABEL	9