PRO-SYS
- Product NDC
- 66975-779
- 11-digit product format
- 669750779
- Labeler code
- 66975
- Product ID
- 66975-779_500d975b-b5ef-fc25-e063-6294a90a8377
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Professional Sensitivity, SLS Free - Mint (5000 ppm)
- Dosage form
- PASTE, DENTIFRICE
- Route
- DENTAL
- Labeler
- Benco Dental
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2025-12-01
- Substance
- POTASSIUM NITRATE; SODIUM FLUORIDE
- Active strength
- 5; 1.1 g/100g; g/100g
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- PRO-SYS
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| POTASSIUM NITRATE | 5 g/100g |
| SODIUM FLUORIDE | 1.1 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | RU45X2JN0Z, 8ZYQ1474W7 |
| Rxcui | 637365 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 66975-779-01 | PRO-SYS | 113 g in 1 TUBE | PASTE, DENTIFRICE | 113 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 66975-779-01 | 66975077901 | 113 g in 1 TUBE (66975-779-01) | 113 g | 2025-12-01 | No | No | Current |