Pro-Den Rx
- Product NDC
- 59883-912
- 11-digit product format
- 598830912
- Labeler code
- 59883
- Product ID
- 59883-912_82f91600-bbd0-30d0-e053-2991aa0adf68
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium Fluoride
- Dosage form
- RINSE
- Route
- ORAL
- Labeler
- Den-mat Holdings, Llc
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2008-10-21
- Marketing end
- 0000-00-00
- Substance
- SODIUM FLUORIDE
- Active strength
- 1 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 59883-912-64 | Pro-Den Rx | 1890 mL in 1 BOTTLE, PLASTIC | RINSE | 1890 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 59883-912 | PRO-DEN RX (SODIUM FLUORIDE) RINSE [DEN-MAT HOLDINGS, LLC] | 2 | Legacy NDC, 1 package rows | 20190301_d4235a56-a82b-48f0-b72f-5f0c58f54f26.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 59883-912-64 | 59883091264 | 1890 mL in 1 BOTTLE, PLASTIC (59883-912-64) | 1890 ml | 2008-10-21 | 0000-00-00 | No | No | Current |