NAFRINSE PACKETS BUBBLE GUM
- Product NDC
- 0273-8014
- 11-digit product format
- 002738014
- Labeler code
- 0273
- Product ID
- 0273-8014_ef864e8e-21b8-44a6-a69f-09162db3018d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium Fluoride
- Dosage form
- POWDER
- Route
- DENTAL
- Labeler
- Young Dental Manufacturing Co 1, LLC.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2017-09-21
- Marketing end
- 0000-00-00
- Substance
- SODIUM FLUORIDE
- Active strength
- 1 g/g
- 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 |
|---|
| 0273-8014-02 | NAFRINSE PACKETS BUBBLE GUM | 2 g in 1 PACKET | POWDER | 2 | | 2 |
| 0273-8014-02 | NAFRINSE PACKETS BUBBLE GUM | 50 in 1 PACKAGE | POWDER | 50 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0273-8014 | NAFRINSE PACKETS BUBBLE GUM (SODIUM FLUORIDE) POWDER [YOUNG DENTAL MANUFACTURING CO 1, LLC.] | 2 | Legacy NDC, 2 package rows | 20181215_b1905e1a-e776-44eb-8658-2e6965d842e8.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 0273-8014-02 | 00273801402 | 2 g in 1 PACKET | 2 g | Historical |