NDC codes

FDA NDC Directory
Product NDC (as listed)88118-001Labeler and product segments. Claims need a package NDC.
Product NDC at billing width88118-0001Add 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
88118-001-0488118000104881180001041 BOTTLE in 1 BOX (88118-001-04) / 120 mL in 1 BOTTLEMarketed from Oct 29, 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

Generic name (nonproprietary)
sodium chloride
Active ingredients
Sodium chloride — 9 mg/mL
Dosage form
Solution
Route
Cutaneous, Nasal, Ophthalmic, Topical
Labeler
BIOLOGIX USA, INC.NDC labeler code 88118
Product type
Over-the-counter drug
Marketing category
Unapproved drug (other)
Marketing start
Listing expires
Identifiers
Product ID 88118-001_5edb1f1e-122e-f0da-e063-6394a90a4ccdSPL ID 5edb1f1e-122e-f0da-e063-6394a90a4ccdSPL set ID 5edb1f1e-122d-f0da-e063-6394a90a4ccdRxCUI 199266, 313000, 2706648UNII 451W47IQ8XUPC 0860016515642

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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

NDC on a medical claim

N488118000104 followed by a unit qualifier and the quantity

Package 88118-0001-04. 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)

This product is designed for gentle cleaning of the face, mouth, nose, eyes, ears, and wounds. It can also be used with a nebulizer to help relieve discomfort in the nose and mouth

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 88118-001

What is NDC 88118-001?
88118-001 is the product NDC for BiologixCare Sterile Saline Wound Wash, Sodium chloride 9 mg/mL solution, listed with the FDA by BIOLOGIX USA, INC.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
BiologixCare Sterile Saline Wound Wash (Sodium Chloride).
What is the active ingredient?
Sodium chloride.
Who is the labeler?
BIOLOGIX USA, INC., NDC labeler code 88118. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for BiologixCare Sterile Saline Wound Wash?
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.

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