NAFRINSE PACKETSKIT Bubble Gum
- Product NDC
- 0273-8008
- 11-digit product format
- 002738008
- Labeler code
- 0273
- Product ID
- 0273-8008_4d09eaa9-531c-47d9-83f5-c4286cff99df
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium Fluoride
- Dosage form
- POWDER
- Route
- DENTAL
- Labeler
- Young Dental Manufacturing I, LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2017-09-25
- 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 |
|---|
| 0273-8008-01 | NAFRINSE PACKETSKIT Bubble Gum | 3 g in 1 PACKET | POWDER | 3 | | 2 |
| 0273-8008-02 | NAFRINSE PACKETSKIT Bubble Gum | 20 in 1 KIT | POWDER | 20 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0273-8008 | NAFRINSE PACKETSKIT BUBBLE GUM (SODIUM FLUORIDE) POWDER [YOUNG DENTAL MANUFACTURING I, LLC] | 2 | Legacy NDC, 2 package rows | 20181215_4ca4be4a-6590-465f-be63-ee50bd421748.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 0273-8008-01 | 00273800801 | 3 g in 1 PACKET | 3 g | Historical |
| 0273-8008-02 | 00273800802 | 20 in 1 KIT | | Historical |