NAFRINSE UNIT DOSE FLUORIDE
- Product NDC
- 0273-8001
- 11-digit product format
- 002738001
- Labeler code
- 0273
- Product ID
- 0273-8001_2ba94fad-a133-4af0-8129-721741f6f949
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium Fluoride
- Dosage form
- SOLUTION
- Route
- DENTAL
- Labeler
- Young Dental Manufacturing Co 1, LLC.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2017-09-24
- Marketing end
- 0000-00-00
- Substance
- SODIUM FLUORIDE
- Active strength
- 20 mg/10mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0273-8001-01 | NAFRINSE UNIT DOSE FLUORIDE | 10 mL in 1 CUP | SOLUTION | 10 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0273-8001 | NAFRINSE UNIT DOSE FLUORIDE (SODIUM FLUORIDE) SOLUTION [YOUNG DENTAL MANUFACTURING CO 1, LLC.] | 2 | Legacy NDC, 1 package rows | 20181215_8eeaca73-0a28-4cbd-901d-cfc278ef1a9f.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 0273-8001-01 | 00273800101 | 10 mL in 1 CUP | 10 ml | Historical |