Sodium Fluoride 5000 PPM
- Product NDC
- 69367-311
- 11-digit product format
- 693670311
- Labeler code
- 69367
- Product ID
- 69367-311_f227132c-6257-4245-b8e0-7de78c15c201
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium Fluoride
- Dosage form
- PASTE
- Route
- DENTAL
- Labeler
- Westminster Pharmaceuticals, LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2021-06-16
- Substance
- SODIUM FLUORIDE
- Active strength
- 6 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Sodium Fluoride 5000 PPM
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM FLUORIDE | 6 mg/mL |
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 |
|---|
| 69367-311-01 | Sodium Fluoride 5000 PPM | 100 mL in 1 TUBE | PASTE | 100 | | 9 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69367-311 | SODIUM FLUORIDE 5000 PPM (SODIUM FLUORIDE) PASTE [WESTMINSTER PHARMACEUTICALS, LLC] | 9 | Current NDC, Legacy NDC, 1 package rows | 20250417_56efb346-c715-463d-9260-f7fcfbd2b70f.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69367-311-01 | 69367031101 | 100 mL in 1 TUBE (69367-311-01) | 100 ml | 2021-06-16 | 0000-00-00 | No | No | Current |