DOCTRUST K Tooth
NDC 76670-0014, Silicon dioxide, Sodium monofluorophosphate, gel, dentifrice, from DOCSMEDI Co., Ltd..
- Product NDC
- 76670-0014
- Status
- Listed
- Labeler
- DOCSMEDI Co., Ltd.
- Dosage form
- GEL, DENTIFRICE
- Route
- DENTAL
- Product type
- HUMAN OTC DRUG
- Marketing category
- UNAPPROVED DRUG OTHER
- Application
- —
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/76670-0014 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SILICON DIOXIDE16 g/100g
- SODIUM MONOFLUOROPHOSPHATE.74 g/100g
| Package NDC | NDC-11 | Package |
|---|---|---|
| 76670-0014-2 | 76670001402 | 1 TUBE in 1 CARTON (76670-0014-2) / 60 g in 1 TUBE (76670-0014-1) |
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 76670-0014 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/76670-0014 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 76670-0014. 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.