Pro-Den Rx
- Product NDC
- 59883-720
- 11-digit product format
- 598830720
- Labeler code
- 59883
- Product ID
- 59883-720_0a95fcbe-e811-031d-e063-6294a90aec1b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Stannous Fluoride
- Dosage form
- RINSE
- Route
- ORAL
- Labeler
- Den-mat Holdings, Llc
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2008-10-31
- Substance
- STANNOUS FLUORIDE
- Active strength
- 1.53 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Pro-Den Rx
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| STANNOUS FLUORIDE | 1.53 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3FTR44B32Q |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 59883-720-08 | Pro-Den Rx | 283.5 g in 1 BOTTLE | RINSE | 283.5 | | 6 |
| 59883-720-08 | Pro-Den Rx | 1 in 1 CARTON | RINSE | 1 | | 6 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 59883-720 | PRO-DEN RX (STANNOUS FLUORIDE) RINSE [DEN-MAT HOLDINGS, LLC] | 6 | Current NDC, Legacy NDC, 2 package rows | 20231216_9036aa8a-59b1-41b0-b3cb-529d3303a1c0.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 59883-720-08 | 59883072008 | 1 BOTTLE in 1 CARTON (59883-720-08) / 283.5 g in 1 BOTTLE | 1 bottle | 2008-10-31 | 0000-00-00 | No | No | Current |