Sensodyne
- Product NDC
- 0135-4032
- 11-digit product format
- 001354032
- Labeler code
- 0135
- Product ID
- 0135-4032_445ed08a-b479-1982-e063-6394a90a6cc3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- potassium nitrate, sodium fluoride
- Dosage form
- PASTE, DENTIFRICE
- Route
- DENTAL
- Labeler
- Haleon US Holdings LLC
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-12-15
- Substance
- POTASSIUM NITRATE; SODIUM FLUORIDE
- Active strength
- 50; 1.5 mg/g; mg/g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| RU45X2JN0Z | POTASSIUM NITRATE | 7757-79-1 | POTASSIUM NITRATE |
| 8ZYQ1474W7 | SODIUM FLUORIDE | 7681-49-4 | SODIUM FLUORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 0135-4032-01 | 00135403201 | 1 TUBE in 1 CARTON (0135-4032-01) / 77 g in 1 TUBE | 1 tube | 2025-12-15 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Drug Facts | Haleon US Holdings LLC | 2025-11-24 | HUMAN OTC DRUG LABEL | 1 |