NDC codes

FDA NDC Directory
Product NDC (as listed)73492-281Labeler and product segments. Claims need a package NDC.
Product NDC at billing width73492-0281Add 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 NDC11-digit (billing)PackageCopy
73492-281-04734920281047349202810444 mL in 1 BOTTLE, SPRAY (73492-281-04)Marketed from Jun 19, 2026
73492-281-09734920281097349202810990 mL in 1 BOTTLE, SPRAY (73492-281-09)Marketed from Jul 6, 2026

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)
Saline Nasal
Generic name (nonproprietary)
sodium chloride
Active ingredients
Sodium chloride — 6.5 mg/mL
Dosage form
Spray
Route
Nasal
Labeler
ALAINA HEALTHCARE PRIVATE LIMITEDNDC labeler code 73492
Product type
Over-the-counter drug
Marketing category
OTC monograph drugApplication M 022
Marketing start
Listing expires
Identifiers
Product ID 73492-281_56038b75-6518-9302-e063-6394a90a0e21SPL ID 56038b75-6518-9302-e063-6394a90a0e21SPL set ID ed30a7f9-7132-42da-9bed-63a9b1c80ab2RxCUI 707251UNII 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

N473492028104 followed by a unit qualifier and the quantity

Package 73492-0281-04. 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 .

Indications (excerpt from the label)

Uses provides moisture to dry nasal passages helps relieve dry, irritated nasal passages due to colds, allergies, dry air, pollution, smoke, air travel, and use of decongestants/steroidal sprays.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 73492-281

What is NDC 73492-281?
73492-281 is the product NDC for Saline Nasal (sodium chloride), Sodium chloride 6.5 mg/mL spray, listed with the FDA by ALAINA HEALTHCARE PRIVATE LIMITED. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Saline Nasal (Sodium chloride).
What is the active ingredient?
Sodium chloride.
Who is the labeler?
ALAINA HEALTHCARE PRIVATE LIMITED, NDC labeler code 73492. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Saline 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 022

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

FDA NDC Directory listings under M 022
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Walgreens Maximum StrengthbenzocaineBenzocaine 20 g/100gPaste, DentifriceTopicalWalgreens0363-5337
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Dem Zerophosphatidylserine, magnesium oxidePhosphatidyl serine 214.43 mg/450mg + 2 more ingredientsTabletOralNPG Bio Pharmaceuticals Co.,Ltd.84540-240
Benzoin Tincturebenzoin resinBenzoin resin 1000 mg/mLLiquidTopical11695664470677-1200
Rite Aid Maximum StrengthbenzocaineBenzocaine 20 g/100gLiquidOralRite Aid11822-0345
Chloraseptic Sore Throat CitrusphenolPhenol 1.4 g/100mLSprayOralPrestige Brands Holdings, Inc.67172-112
Sore Throat Relief Cherry FlavorphenolPhenol 1.4 g/100mLSprayOralCardinal Health70000-0458
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Rite Aid Professional StrengthbenzocaineBenzocaine 20 g/100gLiquidOralRite Aid11822-5340
Benzocaine 20%Benzocaine 200 mg/mLSolutionTopicalPAI Holdings, LLC dba PAI Pharma0121-1077

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