DENTI BUONGIORNO GUM CARE TOOTH
NDC 73242-1118, Silica, Sodium Fluoride, Tocopheryl Acetate, paste, dentifrice, from DONG IL PHARMS CO.,LTD.
- Product NDC
- 73242-1118
- Status
- Listed
- Labeler
- DONG IL PHARMS 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/73242-1118 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- .ALPHA.-TOCOPHEROL ACETATE.2 g/100g
- SILICON DIOXIDE15 g/100g
- SODIUM FLUORIDE.22 g/100g
| Package NDC | NDC-11 | Package |
|---|---|---|
| 73242-1118-2 | 73242111802 | 1 TUBE in 1 CARTON (73242-1118-2) / 100 g in 1 TUBE (73242-1118-1) |
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 73242-1118 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/73242-1118 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 73242-1118. 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.