Prosys
- Product NDC
- 66975-782
- 11-digit product format
- 669750782
- Labeler code
- 66975
- Product ID
- 66975-782_500d9ff5-0091-fc40-e063-6394a90a8810
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- 1.1% Sodium Fluoride
- Dosage form
- PASTE, DENTIFRICE
- Route
- DENTAL
- Labeler
- Benco Dental
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2026-02-01
- Substance
- SODIUM FLUORIDE
- Active strength
- .11 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
- Prosys
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM FLUORIDE | .11 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 8ZYQ1474W7 |
| Rxcui | 392038 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 66975-782-01 | Prosys | 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 |
|---|
| 66975-782-01 | 66975078201 | 113 g in 1 TUBE (66975-782-01) | 113 g | 2026-02-01 | No | No | Current |