NDC codes

FDA NDC Directory
Product NDC (as listed)73242-1128Labeler and product segments. Claims need a package NDC.
Product NDC at billing width73242-1128Add 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
73242-1128-273242112802732421128021 TUBE in 1 CARTON (73242-1128-2) / 100 g in 1 TUBE (73242-1128-1)Marketed from Jan 2, 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

Generic name (nonproprietary)
silica, sodium monofluorophosphate
Active ingredients
Silicon dioxide — 18 g/100gSodium monofluorophosphate — .76 g/100g
Dosage form
Paste, Dentifrice
Route
Oral
Labeler
DONG IL PHARMS CO.,LTDNDC labeler code 73242
Product type
Over-the-counter drug
Marketing category
Unapproved drug (other)
Marketing start
Listing expires
Identifiers
Product ID 73242-1128_487d9d48-6b2c-8a64-e063-6294a90a732eSPL ID 487d9d48-6b2c-8a64-e063-6294a90a732eSPL set ID 487da363-1d01-8cdc-e063-6294a90ac24dRxCUI 2732211UNII ETJ7Z6XBU4, C810JCZ56Q

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. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N473242112802 followed by a unit qualifier and the quantity

Package 73242-1128-02. 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 .

Indications (excerpt from the label)

Use(s) • Helps remove plaque and tartar buildup • Helps prevent cavities • Helps reduce gum inflammation and promote healthy teeth

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 73242-1128

What is NDC 73242-1128?
73242-1128 is the product NDC for Denti Buongiorno Fresh Breath Herb Mint Tooth, Silicon dioxide 18 g/100g; Sodium monofluorophosphate .76 g/100g paste, dentifrice, listed with the FDA by DONG IL PHARMS CO.,LTD. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Denti Buongiorno Fresh Breath Herb Mint Tooth (Silica, Sodium Monofluorophosphate).
What is the active ingredient?
Silicon dioxide, Sodium monofluorophosphate.
Who is the labeler?
DONG IL PHARMS CO.,LTD, NDC labeler code 73242. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Denti Buongiorno Fresh Breath Herb Mint Tooth?
1 other product NDC are listed under this name. See all Denti Buongiorno Fresh Breath Herb Mint Tooth 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 Denti Buongiorno Fresh Breath Herb Mint Tooth NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Denti Buongiorno Fresh Breath Herb Mint Toothsilica, sodium monofluorophosphateSilicon dioxide 18 g/100g; Sodium monofluorophosphate .76 g/100gPaste, DentifriceOralATOSAFE CO., Ltd85601-11085601-0110-02

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