Native
- Product NDC
- 69423-903
- 11-digit product format
- 694230903
- Labeler code
- 69423
- Product ID
- 69423-903_f1ed4a45-46d4-fca9-e053-2a95a90a7023
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Potassium Nitrate, Sodium Fluoride
- Dosage form
- PASTE, DENTIFRICE
- Route
- DENTAL
- Labeler
- The Procter & Gamble Manufacturing Company
- Application
- part356
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2021-05-10
- Marketing end
- 0000-00-00
- Substance
- POTASSIUM NITRATE; SODIUM FLUORIDE
- Active strength
- 50 mg/g; mg/g
- NDC exclude flag
- No
- Listing certified through
- 2024-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded product | product | 69423-903 | D | Discontinued by firm | 2026-10-05 | ||
| excluded package | package | 69423-903 | 69423-903-41 | D | Discontinued by firm | 2026-10-05 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Dashboard NDC Coverage#
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 69423-903-41 | 69423090341 | 1 TUBE in 1 CARTON (69423-903-41) > 116 g in 1 TUBE | 1 tube | 2021-05-10 | 0000-00-00 | No | No | Current |