NDC codes

FDA NDC Directory
Product NDC (as listed)69367-309Labeler and product segments. Claims need a package NDC.
Product NDC at billing width69367-0309Add 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
69367-309-51693670309511 TUBE in 1 CARTON (69367-309-51) / 51 g in 1 TUBEMarketed from Mar 9, 2021

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)
Sodium Fluoride 5000 Plus
Generic name (nonproprietary)
sodium fluoride
Active ingredients
Sodium fluoride — 5 mg/g
Dosage form
Cream
Route
Dental
Labeler
Westminster Pharmaceuticals, LLCNDC labeler code 69367
Product type
Prescription drug
Marketing category
Unapproved drug (other)
Marketing start
Listing expires
Identifiers
Product ID 69367-309_332a3cc9-03d0-4e9e-ab80-f597b4198aa0SPL ID 332a3cc9-03d0-4e9e-ab80-f597b4198aa0

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

N469367030951 followed by a unit qualifier and the quantity

Package 69367-0309-51. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 69367-309

What is NDC 69367-309?
69367-309 is the product NDC for Sodium Fluoride 5000 Plus (sodium fluoride), Sodium fluoride 5 mg/g cream, listed with the FDA by Westminster Pharmaceuticals, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Sodium Fluoride 5000 Plus (Sodium Fluoride).
What is the active ingredient?
Sodium fluoride.
Who is the labeler?
Westminster Pharmaceuticals, LLC, NDC labeler code 69367. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Sodium Fluoride 5000 Plus?
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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