DENTI BUONGIORNO ORIGINAL TOOTH
NDC 85601-050, Silica, Sodium Monofluorophosphate, paste, dentifrice, from ATOSAFE CO., Ltd.
- Product NDC
- 85601-050
- Status
- Listed
- Labeler
- ATOSAFE CO., Ltd
- Dosage form
- PASTE, DENTIFRICE
- Route
- ORAL
- Product type
- HUMAN OTC DRUG
- Marketing category
- UNAPPROVED DRUG OTHER
- Application
- —
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/85601-050 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SILICON DIOXIDE18 g/100g
- SODIUM MONOFLUOROPHOSPHATE.76 g/100g
| Package NDC | NDC-11 | Package |
|---|---|---|
| 85601-050-02 | 85601005002 | 1 TUBE in 1 CARTON (85601-050-02) / 100 g in 1 TUBE (85601-050-01) |
Linked data
RxNorm, label and prices
RxNorm concepts
RxNorm links no concept to this product's packages.
Related lookups
No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.
Use it
Look up 85601-050 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/85601-050 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 85601-050. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.