What is NDC 51672-1405?

51672-1405 is the product NDC for Oxymetazoline Hydrochloride, Oxymetazoline hydrochloride 10 mg/g cream, listed with the FDA by Sun Pharmaceutical Industries, Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.

Sun Pharmaceutical Industries, Inc., NDC labeler code 51672. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Oxymetazoline Hydrochloride?

7 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Oxymetazoline Hydrochloride NDC 51672-1405

NDC codes

FDA NDC Directory

Product NDC (as listed)51672-1405Labeler and product segments. Claims need a package NDC.

Product NDC at billing width51672-1405Add 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
51672-1405-2	51672140502	1 TUBE in 1 CARTON (51672-1405-2) / 30 g in 1 TUBEMarketed from Jul 15, 2026
51672-1405-3	51672140503	1 TUBE in 1 CARTON (51672-1405-3) / 60 g in 1 TUBEMarketed from Jul 15, 2026

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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): Oxymetazoline Hydrochloride
Generic name (nonproprietary): oxymetazoline hydrochloride
Active ingredients: Oxymetazoline hydrochloride — 10 mg/g
Dosage form: Cream
Route: Topical
Labeler: Sun Pharmaceutical Industries, Inc.NDC labeler code 51672
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 213584
Marketing start: Jul 15, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Imidazolines (Chemical structure)Increased Sympathetic Activity (Physiologic effect)Vasoconstriction (Physiologic effect)
Identifiers: Product ID 51672-1405_5151bebc-ad61-adae-e063-6394a90a2720SPL ID 5151bebc-ad61-adae-e063-6394a90a2720SPL set ID 8a7f2400-5e18-4215-8d2c-f55881706107RxCUI 1869816UNII 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. Topical products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N451672140502 followed by a unit qualifier and the quantity

Package 51672-1405-02. 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 May 8, 2026.

Indications (excerpt from the label)

Oxymetazoline hydrochloride cream is indicated for the topical treatment of persistent facial erythema associated with rosacea in adults. Oxymetazoline hydrochloride cream is an alpha 1A adrenoceptor agonist indicated for the topical treatment of persistent facial erythema associated with rosacea in adults. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 51672-1405

What is NDC 51672-1405?: 51672-1405 is the product NDC for Oxymetazoline Hydrochloride, Oxymetazoline hydrochloride 10 mg/g cream, listed with the FDA by Sun Pharmaceutical Industries, Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Oxymetazoline Hydrochloride.
What is the active ingredient?: Oxymetazoline hydrochloride.
Who is the labeler?: Sun Pharmaceutical Industries, Inc., NDC labeler code 51672. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Oxymetazoline Hydrochloride?: 7 other product NDCs are listed under this name. See all Oxymetazoline Hydrochloride NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Oxymetazoline Hydrochloride NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Oxymetazoline hydrochloride	Oxymetazoline hydrochloride .05 g/100mL	SprayNasal	Prodose, Inc.	68210-5056	68210-5056-01
Oxymetazoline Hydrochloride	Oxymetazoline hydrochloride .05 g/100mL	SprayNasal	Bi-Mart	37835-996	37835-0996-01
Oxymetazoline Hydrochloride	Oxymetazoline hydrochloride .05 mg/mL	SolutionNasal	CHAIN DRUG MARKETING ASSOCIATION INC	63868-608	63868-0608-01
Oxymetazoline Hydrochloride	Oxymetazoline hydrochloride .05 g/100mL	SprayNasal	CHAIN DRUG MARKETING ASSOCIATION INC.	63868-605	63868-0605-01
Oxymetazoline Hydrochloride	Oxymetazoline hydrochloride .05 g/100mL	SprayNasal	CHAIN DRUG MARKETING ASSOCIATION INC.	63868-607	63868-0607-01
Oxymetazoline Hydrochloride	Oxymetazoline hydrochloride .05 g/100mL	SprayNasal	CHAIN DRUG MARKETING ASSOCIATION INC.	63868-676	63868-0676-01
oxymetazoline hydrochloride	Oxymetazoline hydrochloride .05 g/100mL	SprayNasal	NuCare Pharmaceuticals,Inc.	68071-3422	68071-3422-01