NDC codes

FDA NDC Directory
Product NDC (as listed)73242-1127Labeler and product segments. Claims need a package NDC.
Product NDC at billing width73242-1127Add 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
73242-1127-273242112702732421127021 TUBE in 1 CARTON (73242-1127-2) / 100 g in 1 TUBE (73242-1127-1)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 fluoride, tocopheryl acetate
Active ingredients
.alpha.-tocopherol acetate — .2 g/100gSodium fluoride — .22 g/100gSilicon dioxide — 15 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 73242-1127_487d73be-0ff9-f417-e063-6394a90a0668SPL ID 487d73be-0ff9-f417-e063-6394a90a0668SPL set ID 487d689d-ebdd-43c3-e063-6294a90af0e2RxCUI 2713755UNII 9E8X80D2L0, 8ZYQ1474W7, ETJ7Z6XBU4

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

N473242112702 followed by a unit qualifier and the quantity

Package 73242-1127-02. 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 73242-1127

What is NDC 73242-1127?
73242-1127 is the product NDC for Denti Buongiorno Gum Care Cool Mint Tooth, .alpha.-tocopherol acetate .2 g/100g + 2 more ingredients 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 Gum Care Cool Mint Tooth (Silica, Sodium Fluoride, Tocopheryl Acetate).
What is the active ingredient?
.alpha.-tocopherol acetate, Sodium fluoride, Silicon dioxide.
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 Gum Care Cool Mint Tooth?
1 other product NDC are listed under this name. See all Denti Buongiorno Gum Care Cool 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 Gum Care Cool Mint Tooth NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Denti Buongiorno Gum Care Cool Mint Toothsilica, sodium fluoride, tocopheryl acetate.alpha.-tocopherol acetate .2 g/100g + 2 more ingredientsPaste, DentifriceOralATOSAFE CO., Ltd85601-10085601-0100-02

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