NDC codes

FDA NDC Directory
Product NDC (as listed)76670-0014Labeler and product segments. Claims need a package NDC.
Product NDC at billing width76670-0014Add 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
76670-0014-276670001402766700014021 TUBE in 1 CARTON (76670-0014-2) / 60 g in 1 TUBE (76670-0014-1)Marketed from Dec 1, 2022

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

Brand name (proprietary)
DOCTRUST K Tooth
Generic name (nonproprietary)
silicon dioxide, sodium monofluorophosphate
Active ingredients
Silicon dioxide — 16 g/100gSodium monofluorophosphate — .74 g/100g
Dosage form
Gel, Dentifrice
Route
Dental
Labeler
DOCSMEDI Co., Ltd.NDC labeler code 76670
Product type
Over-the-counter drug
Marketing category
Unapproved drug (other)
Marketing start
Listing expires
Identifiers
Product ID 76670-0014_2c484532-89d7-c8d3-e063-6294a90a793dSPL ID 2c484532-89d7-c8d3-e063-6294a90a793dSPL set ID a02f8865-e7be-4ef4-b09c-dad846639764UNII ETJ7Z6XBU4, C810JCZ56QUPC 8809805370170

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

N476670001402 followed by a unit qualifier and the quantity

Package 76670-0014-02. 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)

Uses ■ Helps protect against cavities

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 76670-0014

What is NDC 76670-0014?
76670-0014 is the product NDC for DOCTRUST K Tooth, Silicon dioxide 16 g/100g; Sodium monofluorophosphate .74 g/100g gel, dentifrice, listed with the FDA by DOCSMEDI Co., Ltd.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
DOCTRUST K Tooth (Silicon dioxide, Sodium monofluorophosphate).
What is the active ingredient?
Silicon dioxide, Sodium monofluorophosphate.
Who is the labeler?
DOCSMEDI Co., Ltd., NDC labeler code 76670. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for DOCTRUST K Tooth?
1 other product NDC are listed under this name. See all DOCTRUST K 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 DOCTRUST K Tooth NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
DOCTRUST K Toothsilicon dioxide, sodium monofluorophosphateSilicon dioxide 16 g/100g; Sodium monofluorophosphate .74 g/100gGel, DentifriceDentalDONG IL PHARMS CO.,LTD73242-112373242-1123-02

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