What is NDC 73024-474?

73024-474 is the product NDC for Rhinomel Manuka (sodium chloride), Sodium chloride 9 mg/mL spray, listed with the FDA by Melcare Biomedical Pty Ltd. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Rhinomel Manuka (Sodium chloride).

Melcare Biomedical Pty Ltd, NDC labeler code 73024. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Rhinomel Manuka?

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.

Rhinomel Manuka NDC 73024-474 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)73024-474Labeler and product segments. Claims need a package NDC.

Product NDC at billing width73024-0474Add 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
73024-474-10	7302404741073024047410	1 BOTTLE, SPRAY in 1 CARTON (73024-474-10) / 20 mL in 1 BOTTLE, SPRAYMarketed from May 21, 2025

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): Rhinomel Manuka
Generic name (nonproprietary): sodium chloride
Active ingredients: Sodium chloride — 9 mg/mL
Dosage form: Spray
Route: Nasal
Labeler: Melcare Biomedical Pty LtdNDC labeler code 73024
Product type: Over-the-counter drug
Marketing category: Unapproved drug (other)
Marketing start: May 21, 2025
Listing expires: Dec 31, 2026
Identifiers: Product ID 73024-474_458a65a1-575a-a14d-e063-6294a90ace39SPL ID 458a65a1-575a-a14d-e063-6294a90ace39SPL set ID 35a7ce7d-4a26-e3f0-e063-6294a90ad66fRxCUI 351179, 2714714UNII 451W47IQ8X

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

N473024047410 followed by a unit qualifier and the quantity

Package 73024-0474-10. 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 Dec 9, 2025.

Indications (excerpt from the label)

Use s For persons prone to congestion

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 73024-474

What is NDC 73024-474?: 73024-474 is the product NDC for Rhinomel Manuka (sodium chloride), Sodium chloride 9 mg/mL spray, listed with the FDA by Melcare Biomedical Pty Ltd. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Rhinomel Manuka (Sodium chloride).
What is the active ingredient?: Sodium chloride.
Who is the labeler?: Melcare Biomedical Pty Ltd, NDC labeler code 73024. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Rhinomel Manuka?: 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.

Rhinomel Manuka (Sodium chloride) NDC 73024-474