What is NDC 11673-304?

11673-304 is the product NDC for Up and up nasal (oxymetazoline hydrochloride), Oxymetazoline hydrochloride .05 g/100mL spray, listed with the FDA by Target Corporation. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Up and up nasal (Oxymetazoline hydrochloride).

Target Corporation, NDC labeler code 11673. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Up and up nasal?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Up and up nasal NDC 11673-304 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)11673-304Labeler and product segments. Claims need a package NDC.

Product NDC at billing width11673-0304Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
11673-304-10	11673030410	1 BOTTLE, SPRAY in 1 CARTON (11673-304-10) / 30 mL in 1 BOTTLE, SPRAYMarketed from Aug 12, 2009

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Up and up nasal
Generic name (nonproprietary): oxymetazoline hydrochloride
Active ingredients: Oxymetazoline hydrochloride — .05 g/100mL
Dosage form: Spray
Route: Nasal
Labeler: Target CorporationNDC labeler code 11673
Product type: Over-the-counter drug
Marketing category: OTC monograph drugApplication M 012
Marketing start: Aug 12, 2009
Listing expires: Dec 31, 2026
Other FDA classes: Imidazolines (Chemical structure)Increased Sympathetic Activity (Physiologic effect)Vasoconstriction (Physiologic effect)
Identifiers: Product ID 11673-304_9211198c-c1b8-493d-b7ee-3a9073815388SPL ID 9211198c-c1b8-493d-b7ee-3a9073815388SPL set ID 0c246c11-eadd-4ac6-bd58-5fdb151e06d6RxCUI 1000990UNII K89MJ0S5VY
Pharmacologic class: Vasoconstrictor

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Nasal products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N411673030410 followed by a unit qualifier and the quantity

Package 11673-0304-10. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Sep 4, 2024.

Indications (excerpt from the label)

Uses • temporarily relieves nasal congestion due to: • common cold • hay fever • upper respiratory allergies • temporarily relieves sinus congestion and pressure • shrinks swollen nasal membranes so you can breathe more freely

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 11673-304

What is NDC 11673-304?: 11673-304 is the product NDC for Up and up nasal (oxymetazoline hydrochloride), Oxymetazoline hydrochloride .05 g/100mL spray, listed with the FDA by Target Corporation. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Up and up nasal (Oxymetazoline hydrochloride).
What is the active ingredient?: Oxymetazoline hydrochloride.
Who is the labeler?: Target Corporation, NDC labeler code 11673. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Up and up nasal?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other NDCs under M 012

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under M 012
Product	Strength	Form · route	Labeler	Product NDC
12 Hour Nasal Decongestant Extra Moisturizingnasal spray	Oxymetazoline hydrochloride 50 mg/100mL	LiquidNasal	WinCo Foods LLC	67091-377
12 Hour Original Nasal Decongestantnasal spray	Oxymetazoline hydrochloride 50 mg/100mL	LiquidNasal	Sheffield Pharmaceuticals LLC	11527-140
12 Hour Original Nasal Decongestantnasal spray	Oxymetazoline hydrochloride 50 mg/100mL	LiquidNasal	WinCo Foods LLC	67091-378
24-7 Life BY 7-ELEVEN Nighttime Cold and Fluacetaminophen, dextromethorphan hbr, doxylamine succinate solution	Dextromethorphan hydrobromide 30 mg/30mL + 2 more ingredients	SolutionOral	Lil' Drug Store products, Inc.	66715-6416
24/7 Life Medicated Chest Rubcamphor, eucalyptus oil, menthol ointment	Eucalyptus oil 1.2 g/100g + 2 more ingredients	OintmentTopical	Lil' Drug Store Products, Inc.	29485-6536
4 Way Fast Actingphenylephrine hydrochloride	Phenylephrine hydrochloride 10 mg/mL	SprayNasal	Haleon US Holdings LLC	0067-2086
7 Select Maximum Strengthdextromethorphan hbr, guaifenesin	Dextromethorphan hydrobromide 20 mg/20mL; Guaifenesin 400 mg/20mL	SolutionOral	7-ELEVEN	10202-740
Acetaminophen 325 mg, Dextromethorphan Hydrobromide 10 mg, Phenlyephrine Hydrochloride 5 mg softgel (DAY-TIME)acetaminophen, dextromethorphan hydrobromide, phenylephrine hydrochloride	Acetaminophen 325 mg/1 + 2 more ingredients	Capsule, Liquid filledOral	Health Pharma USA LLC	71679-101
Acetaminophen 325mg, Dextromethorphan HBr 10mg and Phenyleprine Hcl 5mgacetaminophen, dextromethorphan hbr and phenylephrine hcl	Phenylephrine hydrochloride 5 mg/1 + 2 more ingredients	Capsule, Liquid filledOral	Softgel Healthcare Private Limited	35916-0188
Acetaminophen and Diphenhydramine citrate	Acetaminophen 500 mg/1; Diphenhydramine citrate 38 mg/1	TabletOral	InvaTech Pharma Solutions LLC	57631-010
Acetaminophen PM Extra Strengthacetaminophen, diphenhydramine hcl	Acetaminophen 500 mg/1; Diphenhydramine hydrochloride 25 mg/1	Tablet, CoatedOral	United Natural Foods, Inc. dba UNFI	41163-228
Acetaminophen, Chlorpheniramine Maleate, Dextromethorphan HBr	—	KitOral	CVS Pharmacy, Inc	51316-984
Acetaminophen, Chlorpheniramine Maleate, Phenylephrine HCl	Acetaminophen 500 mg/1 + 2 more ingredients	TabletOral	OPMX LLC	69729-122
Acetaminophen, Chlorpheniramine Maleate, Phenylephrine HCl	Acetaminophen 500 mg/1 + 2 more ingredients	TabletOral	OPMX LLC	69729-322
Acetaminophen, Dextromethorphan HBr	Acetaminophen 325 mg/1; Dextromethorphan hydrobromide 10 mg/1	Capsule, Liquid filledOral	NUVICARE LLC	84324-036
Acetaminophen, Dextromethorphan HBr ,Guaifenesin	Guaifenesin 200 mg/1 + 2 more ingredients	Capsule, Liquid filledOral	Softgel Healthcare Pvt Ltd	35916-0184
Acetaminophen, Dextromethorphan HBr and Doxylamine Succinate	Acetaminophen 325 mg/1 + 2 more ingredients	Capsule, Liquid filledOral	Softgel Healthcare Private Limited	35916-0185
Acetaminophen, Dextromethorphan HBr, Chlorpheniramine Maleate	—	KitOral	CVS Pharmacy, Inc	51316-609
ACETAMINOPHEN, DEXTROMETHORPHAN HBr, GUAILFENESIN,PHENLYEPHRINE HCL	Phenylephrine hydrochloride 5 mg/1 + 3 more ingredients	Capsule, Liquid filledOral	Kroger Company	41226-628
Acetaminophen, Dextromethorphan Hydrobromide and Doxylamine Succinate	Acetaminophen 325 mg/1 + 2 more ingredients	Capsule, Liquid filledOral	Softgel Healthcare Private Limited	35916-0154

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Up and up nasal (Oxymetazoline hydrochloride) NDC 11673-304