sunmark nasal

Product NDC: 49348-130
11-digit product format: 493480130
Labeler code: 49348
Product ID: 49348-130_adb918ac-e3e2-4996-9d6c-c8563df7b05f
Type: HUMAN OTC DRUG
Nonproprietary name: Oxymetazoline HCl
Dosage form: SPRAY
Route: NASAL
Labeler: Strategic Sourcing Services LLC
Application: part341
Marketing category: OTC MONOGRAPH FINAL
Marketing start: 2014-09-26
Marketing end: 0000-00-00
Substance: OXYMETAZOLINE HYDROCHLORIDE
Active strength: 0 g/100mL
NDC exclude flag: No
Listing certified through: 2021-12-31
Current FDA listing: Historical FDA.report record

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 · 2 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded product	product	49348-130		D	Discontinued by firm		2026-10-05
excluded package	package	49348-130	49348-130-27	D	Discontinued by firm		2026-10-05

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 · 12 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
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	49348-130-27	`d630ba8d3edf…`	`732f749b63fb…`
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	49348-130-27	`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	49348-130-27	`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	49348-130-27	`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	49348-130-27	`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	49348-130-27	`cdf11ea48f46…`	`ba0047e9e063…`

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
49348-130-27	ML - Milliliter	49348-130	b4648f48-f791-4e5e-9f50-cca2fb6d8230	1	2015-07-20

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
OXYMETAZOLINE HYDROCHLORIDE	ACTIVE INGREDIENT	K89MJ0S5VY	SUNMARK NASAL (OXYMETAZOLINE HCL) SPRAY [MCKESSON]	1
OXYMETAZOLINE	ACTIVE MOIETY	8VLN5B44ZY	SUNMARK NASAL (OXYMETAZOLINE HCL) SPRAY [MCKESSON]	1
BENZALKONIUM CHLORIDE	INACTIVE INGREDIENT	F5UM2KM3W7	SUNMARK NASAL (OXYMETAZOLINE HCL) SPRAY [MCKESSON]	1
BENZYL ALCOHOL	INACTIVE INGREDIENT	LKG8494WBH	SUNMARK NASAL (OXYMETAZOLINE HCL) SPRAY [MCKESSON]	1
CARBOXYMETHYLCELLULOSE SODIUM	INACTIVE INGREDIENT	K679OBS311	SUNMARK NASAL (OXYMETAZOLINE HCL) SPRAY [MCKESSON]	1
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	SUNMARK NASAL (OXYMETAZOLINE HCL) SPRAY [MCKESSON]	1
EDETATE DISODIUM	INACTIVE INGREDIENT	7FLD91C86K	SUNMARK NASAL (OXYMETAZOLINE HCL) SPRAY [MCKESSON]	1
POLYETHYLENE GLYCOLS	INACTIVE INGREDIENT	3WJQ0SDW1A	SUNMARK NASAL (OXYMETAZOLINE HCL) SPRAY [MCKESSON]	1
POVIDONES	INACTIVE INGREDIENT	FZ989GH94E	SUNMARK NASAL (OXYMETAZOLINE HCL) SPRAY [MCKESSON]	1
SODIUM PHOSPHATE, DIBASIC	INACTIVE INGREDIENT	GR686LBA74	SUNMARK NASAL (OXYMETAZOLINE HCL) SPRAY [MCKESSON]	1
SODIUM PHOSPHATE, MONOBASIC	INACTIVE INGREDIENT	3980JIH2SW	SUNMARK NASAL (OXYMETAZOLINE HCL) SPRAY [MCKESSON]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	SUNMARK NASAL (OXYMETAZOLINE HCL) SPRAY [MCKESSON]	1

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

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
49348-130-27	49348013027	1 BOTTLE, SPRAY in 1 CARTON (49348-130-27) > 30 mL in 1 BOTTLE, SPRAY	2014-09-26	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
McKesson Nasal Spray Drug Facts	Strategic Sourcing Services LLC	2024-08-28	HUMAN OTC DRUG LABEL	5