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NDC 84126-622, Sodium Fluoride and Potassium Nitrate, paste, dentifrice, from The Procter & Gamble Manufacturing Company.
- Product NDC
- 84126-622
- Status
- Listed
- Labeler
- The Procter & Gamble Manufacturing Company
- Dosage form
- PASTE, DENTIFRICE
- Route
- DENTAL
- Product type
- HUMAN OTC DRUG
- Marketing category
- OTC MONOGRAPH DRUG
- Application
- M021
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/84126-622 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- POTASSIUM NITRATE50 mg/g
- SODIUM FLUORIDE1.4 mg/g
| Package NDC | NDC-11 | Package |
|---|---|---|
| 84126-622-06 | 84126062206 | 2 TUBE in 1 CARTON (84126-622-06) / 170 g in 1 TUBE |
| 84126-622-60 | 84126062260 | 1 TUBE in 1 CARTON (84126-622-60) / 170 g in 1 TUBE |
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 84126-622 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/84126-622 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 84126-622. 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.