PreviDent Alcohol Free
NDC 0126-0033, Sodium Fluoride, mouthwash, from Colgate Oral Pharmaceuticals, Inc..
- Product NDC
- 0126-0033
- Status
- Listed
- Labeler
- Colgate Oral Pharmaceuticals, Inc.
- Dosage form
- MOUTHWASH
- Route
- DENTAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- UNAPPROVED DRUG OTHER
- Application
- —
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/0126-0033 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SODIUM FLUORIDE.9 mg/mL
| Package NDC | NDC-11 | Package |
|---|---|---|
| 0126-0033-16 | 00126003316 | 473 mL in 1 BOTTLE, PLASTIC (0126-0033-16) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/28e4f7cd-9fd8-4c7a-9e4b-d747fefc76c0
Use it
Look up 0126-0033 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/0126-0033 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 0126-0033. 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.