Oxymetazoline Hydrochloride

Product NDC: 51672-2030
11-digit product format: 516722030
Labeler code: 51672
Product ID: 51672-2030_56bb5577-e3d4-ae0b-e063-6394a90ab52c
Type: HUMAN OTC DRUG
Nonproprietary name: Oxymetazoline Hydrochloride
Dosage form: SPRAY
Route: NASAL
Labeler: Sun Pharmaceutical Industries, Inc.
Application: M012
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2006-02-25
Substance: OXYMETAZOLINE HYDROCHLORIDE
Active strength: .05 g/100mL
Pharmacologic classes: Imidazolines [CS], Increased Sympathetic Activity [PE], Vasoconstriction [PE], Vasoconstrictor [EPC]
NDC exclude flag: No
Listing certified through: 2027-12-31
Current FDA listing: Yes

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: Oxymetazoline Hydrochloride
Brand name suffix: 12-Hour
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
OXYMETAZOLINE HYDROCHLORIDE	.05 g/100mL

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
34a79f8b-32b7-48db-a895-c942cc795292	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
726062af-1135-4707-a1d7-57256991bbf9	Product name	2	20250226
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
19c71a3d-ed9c-166b-a7e5-38c250c35631	Product name	1	20140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
51672-2030-3	Oxymetazoline Hydrochloride12-Hour	30 mL in 1 BOTTLE, SPRAY	SPRAY	30	3
51672-2030-3	Oxymetazoline Hydrochloride12-Hour	1 in 1 CARTON	SPRAY	1	3
51672-2030-5	Oxymetazoline Hydrochloride12-Hour	15 mL in 1 BOTTLE, SPRAY	SPRAY	15	3
51672-2030-5	Oxymetazoline Hydrochloride12-Hour	1 in 1 CARTON	SPRAY	1	3

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
51672-2030-3	ML - Milliliter	51672-2030	6438d50f-2bf2-4061-a793-5d3f37fb4b61	1	2012-07-24
51672-2030-5	ML - Milliliter	51672-2030	50c5526b-5725-4806-b309-7c4fdb3242e8	1	2012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
OXYMETAZOLINE HYDROCHLORIDE	ACTIVE INGREDIENT	K89MJ0S5VY	OXYMETAZOLINE HYDROCHLORIDE SPRAY, METERED [REBEL DISTRIBUTORS CORP]	2
OXYMETAZOLINE	ACTIVE MOIETY	8VLN5B44ZY	OXYMETAZOLINE HYDROCHLORIDE SPRAY, METERED [REBEL DISTRIBUTORS CORP]	2
BENZALKONIUM CHLORIDE	INACTIVE INGREDIENT	F5UM2KM3W7	OXYMETAZOLINE HYDROCHLORIDE SPRAY, METERED [REBEL DISTRIBUTORS CORP]	2
EDETATE DISODIUM	INACTIVE INGREDIENT	7FLD91C86K	OXYMETAZOLINE HYDROCHLORIDE SPRAY, METERED [REBEL DISTRIBUTORS CORP]	2
POLYETHYLENE GLYCOL 1450	INACTIVE INGREDIENT	OJ4Z5Z32L4	OXYMETAZOLINE HYDROCHLORIDE SPRAY, METERED [REBEL DISTRIBUTORS CORP]	2
POVIDONE	INACTIVE INGREDIENT	FZ989GH94E	OXYMETAZOLINE HYDROCHLORIDE SPRAY, METERED [REBEL DISTRIBUTORS CORP]	2
PROPYLENE GLYCOL	INACTIVE INGREDIENT	6DC9Q167V3	OXYMETAZOLINE HYDROCHLORIDE SPRAY, METERED [REBEL DISTRIBUTORS CORP]	2
SODIUM PHOSPHATE, DIBASIC ANHYDROUS	INACTIVE INGREDIENT	22ADO53M6F	OXYMETAZOLINE HYDROCHLORIDE SPRAY, METERED [REBEL DISTRIBUTORS CORP]	2
SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE	INACTIVE INGREDIENT	593YOG76RN	OXYMETAZOLINE HYDROCHLORIDE SPRAY, METERED [REBEL DISTRIBUTORS CORP]	2
WATER	INACTIVE INGREDIENT	059QF0KO0R	OXYMETAZOLINE HYDROCHLORIDE SPRAY, METERED [REBEL DISTRIBUTORS CORP]	2
Oxymetazoline Hydrochloride	ACTIVE INGREDIENT	K89MJ0S5VY	OXYMETAZOLINE HYDROCHLORIDE 12-HOUR (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [TARO PHARMACEUTICALS U.S.A., INC.]	1
Oxymetazoline	ACTIVE MOIETY	8VLN5B44ZY	OXYMETAZOLINE HYDROCHLORIDE 12-HOUR (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [TARO PHARMACEUTICALS U.S.A., INC.]	1
benzalkonium chloride	INACTIVE INGREDIENT	F5UM2KM3W7	OXYMETAZOLINE HYDROCHLORIDE 12-HOUR (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [TARO PHARMACEUTICALS U.S.A., INC.]	1
edetate disodium	INACTIVE INGREDIENT	7FLD91C86K	OXYMETAZOLINE HYDROCHLORIDE 12-HOUR (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [TARO PHARMACEUTICALS U.S.A., INC.]	1
polyethylene glycol 1450	INACTIVE INGREDIENT	OJ4Z5Z32L4	OXYMETAZOLINE HYDROCHLORIDE 12-HOUR (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [TARO PHARMACEUTICALS U.S.A., INC.]	1
povidone	INACTIVE INGREDIENT	FZ989GH94E	OXYMETAZOLINE HYDROCHLORIDE 12-HOUR (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [TARO PHARMACEUTICALS U.S.A., INC.]	1
propylene glycol	INACTIVE INGREDIENT	6DC9Q167V3	OXYMETAZOLINE HYDROCHLORIDE 12-HOUR (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [TARO PHARMACEUTICALS U.S.A., INC.]	1
sodium phosphate, dibasic, anhydrous	INACTIVE INGREDIENT	22ADO53M6F	OXYMETAZOLINE HYDROCHLORIDE 12-HOUR (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [TARO PHARMACEUTICALS U.S.A., INC.]	1
sodium phosphate, monobasic, monohydrate	INACTIVE INGREDIENT	593YOG76RN	OXYMETAZOLINE HYDROCHLORIDE 12-HOUR (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [TARO PHARMACEUTICALS U.S.A., INC.]	1
water	INACTIVE INGREDIENT	059QF0KO0R	OXYMETAZOLINE HYDROCHLORIDE 12-HOUR (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [TARO PHARMACEUTICALS U.S.A., INC.]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51672-2030	OXYMETAZOLINE HYDROCHLORIDE 12-HOUR (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [TARO PHARMACEUTICALS U.S.A., INC.]	3	Current NDC, Legacy NDC, 4 package rows	20250316_34a79f8b-32b7-48db-a895-c942cc795292.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 112 of 178 · 3,551 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
DayQuil Cold and Flu w/VapoCOOL, 4ct (PE-free), BSX	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE TABLET, COATED	Lil' Drug Store Products, Inc.	37c55543-e05e-2f7c-e063-6394a90a4534	2025-06-20	Warnings	Exact identifier application number: M012
Exchange Select Cough Drops Honey Lemon Sugar-Free	MENTHOL	Xiamen Kang Zhongyuan Biotechnology Co., Ltd.	38049d29-f47e-9478-e063-6294a90aa2a4	2025-06-20	Warnings	Exact identifier application number: M012
Exchange Select Cough Drops Menthol Sugar Free	MENTHOL	Xiamen Kang Zhongyuan Biotechnology Co., Ltd.	3804a271-9a11-848d-e063-6394a90af87d	2025-06-20	Warnings	Exact identifier application number: M012
Exchange Select Cough Drops Menthol Sugar Free	MENTHOL	Army & Air Force Exchange Service	3805ef07-247d-0df7-e063-6394a90ac45b	2025-06-20	Warnings	Exact identifier application number: M012
Exchange Select Cough Drop Black Cherry Sugar Free	MENTHOL	Army & Air Force Exchange Service	3805f8f5-562f-0ba8-e063-6394a90ac9d9	2025-06-20	Warnings	Exact identifier application number: M012
Exchange Select Cough Drops Honey Lemon Sugar-Free	MENTHOL	Army & Air Force Exchange Service	3805f90e-bd89-128d-e063-6394a90afa01	2025-06-20	Warnings	Exact identifier application number: M012
TARGET Multi Symptom Flu Relief	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, AND ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HBR	TARGET CORPORATION	aebe3c15-53ef-46ea-af39-8c9b8114595f	2025-06-20	Warnings	Exact identifier application number: M012
TYLENOL Cold Plus Flu Severe	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE	Morning Star OTC	be95332d-a2e0-42e8-bfb3-8850d74990ff	2025-06-19	Warnings	Exact identifier application number: M012
Tylenol Sinus Severe	ACETAMINOPHEN, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE	Morning Star OTC	37e939c6-064b-3548-e063-6294a90a337d	2025-06-19	Warnings	Exact identifier application number: M012
Capron DM	DEXTROMETHORPHAN HBR AND PYRILAMINE MALEATE	Capital Pharmaceutical, LLC	cf778c5f-475e-4a86-a87c-2be1e665f5a5	2025-06-18	Warnings	Exact identifier application number: M012
Cough Out	GUAIFENESIN	Efficient Laboratories Inc.	fe4c3921-8d30-4cd6-ba90-9211b362a38a	2025-06-18	Warnings	Exact identifier application number: M012
Guaifenesin STRAWBERRY-BANANA FLAVOR	GUAIFENESIN	Innovida Pharmaeutique Corporation	1006906e-d6d7-4f49-92bf-3cb2d2cdbb16	2025-06-18	Warnings	Exact identifier application number: M012
Mucinex Sinus Max Clear and Cool	ACETAMINOPHEN AND GUAIFENESIN	RB Health (US) LLC	37de813a-54b7-672a-e063-6294a90a374e	2025-06-18	Warnings	Exact identifier application number: M012
childrens cold cough	BROMPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE	CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED	4a1aeb41-a8fa-4116-8068-e11acd608e58	2025-06-18	Warnings	Exact identifier application number: M012
NyQuil Cold and Flu w/VapoCOOL, 4ct, Travel BASIX	ACETAMINOPHEN, DOXYLAMINE SUCCINATE, DEXTROMETHORPHAN HYDROBROMIDE TABLET, COATED	Lil' Drug Store Products, Inc.	37c768f5-dabd-22d0-e063-6394a90af9e5	2025-06-17	Warnings	Exact identifier application number: M012
DISCOUNT DRUG MART Childrens Allergy Chewable	DIPHENHYDRAMINE HCL	DISCOUNT DRUG MART	51de95da-e8e8-48f0-9fa4-6191aa4a247b	2025-06-16	Warnings	Exact identifier application number: M012
Halls Cherry	MENTHOL	Mondelez Global LLC	5f4af8e8-8550-45c7-a199-694efac9e7be	2025-06-16	Warnings	Exact identifier application number: M012
Halls Honey Lemon	MENTHOL	Mondelez Global LLC	25eaae85-d516-40da-a472-70736ea2b75d	2025-06-16	Warnings	Exact identifier application number: M012
Halls Cherry	MENTHOL	Mondelez Global LLC	bad89968-22a7-4287-a57c-9e6206e574fe	2025-06-16	Warnings	Exact identifier application number: M012
Herbal Throat Drops	LEMON MINT HERBAL	Meijer, Inc.	37dd58ad-95d1-568c-e063-6394a90a9433	2025-06-16	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	34a79f8b-32b7-48db-a895-c942cc795292	3
1000990	oxymetazoline hydrochloride 0.5 MG/ML Nasal Spray	SCD	34a79f8b-32b7-48db-a895-c942cc795292	3
1000990	oxymetazoline hydrochloride 0.05 % Nasal Spray	SY	34a79f8b-32b7-48db-a895-c942cc795292	3
1000990	oxymetazoline HCl 0.05 % Nasal Spray	PSN	dd196e5a-a791-47ad-aab5-3f2e760f758a	2
1000990	oxymetazoline hydrochloride 0.5 MG/ML Nasal Spray	SCD	dd196e5a-a791-47ad-aab5-3f2e760f758a	2
1000990	oxymetazoline hydrochloride 0.05 % Nasal Spray	SY	dd196e5a-a791-47ad-aab5-3f2e760f758a	2

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
51672-2030-3	51672203003	1 BOTTLE, SPRAY in 1 CARTON (51672-2030-3) / 30 mL in 1 BOTTLE, SPRAY	2006-02-25	0000-00-00	No	No	Current
51672-2030-5	51672203005	1 BOTTLE, SPRAY in 1 CARTON (51672-2030-5) / 15 mL in 1 BOTTLE, SPRAY	2006-02-25	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Oxymetazoline Hydrochloride Nasal Decongestant 12-Hour Spray	Sun Pharmaceutical Industries, Inc. \| Applied Laboratories, Inc.	2026-07-16	HUMAN OTC DRUG LABEL	4
Nasal Decongestant Drug Facts	Rebel Distributors Corp	2011-02-21	HUMAN OTC DRUG LABEL	2