Over-the-counter drug · UNAPPROVED DRUG OTHER
Denti Buongiorno Original Tooth (Silica, sodium monofluorophosphate) NDC 85601-050
Silicon dioxide 18 g/100g; Sodium monofluorophosphate .76 g/100g · Paste, Dentifrice · Oral · ATOSAFE CO., Ltd
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 85601-050-02 | 8560100500285601005002 | 1 TUBE in 1 CARTON (85601-050-02) / 100 g in 1 TUBE (85601-050-01)Marketed from Apr 1, 2025 |
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)
- Denti Buongiorno Original Tooth
- Generic name (nonproprietary)
- silica, sodium monofluorophosphate
- Active ingredients
- Silicon dioxide — 18 g/100gSodium monofluorophosphate — .76 g/100g
- Dosage form
- Paste, Dentifrice
- Route
- Oral
- Labeler
- ATOSAFE CO., LtdNDC labeler code 85601
- Product type
- Over-the-counter drug
- Marketing category
- Unapproved drug (other)
- Marketing start
- Listing expires
- Identifiers
- Product ID 85601-050_4114ab1e-c4ad-5286-e063-6394a90af3cdSPL ID 4114ab1e-c4ad-5286-e063-6394a90af3cdSPL set ID 4114ab09-1115-6b0b-e063-6394a90ab442UNII 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
N485601005002followed by a unit qualifier and the quantityPackage 85601-0050-02. 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) • Fluoride content: 1,000 ppm • Removes plaque (anti-plaque) • Helps reduce bad breath by controlling oral bacteria
Excerpt only. Read the full label for complete information.
About NDC 85601-050
- What is NDC 85601-050?
- 85601-050 is the product NDC for Denti Buongiorno Original Tooth, Silicon dioxide 18 g/100g; Sodium monofluorophosphate .76 g/100g paste, dentifrice, listed with the FDA by ATOSAFE CO., Ltd. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Denti Buongiorno Original Tooth (Silica, Sodium Monofluorophosphate).
- What is the active ingredient?
- Silicon dioxide, Sodium monofluorophosphate.
- Who is the labeler?
- ATOSAFE CO., Ltd, NDC labeler code 85601. 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 Original Tooth?
- 1 other product NDC are listed under this name. See all Denti Buongiorno Original Tooth NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Denti Buongiorno Original Tooth products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Denti Buongiorno Original Toothsilica, sodium monofluorophosphate | Silicon dioxide 18 g/100g; Sodium monofluorophosphate .76 g/100g | Paste, DentifriceOral | DONG IL PHARMS CO.,LTD | 73242-1120 | 73242-1120-02 |