BURST
- Product NDC
- 71275-001
- 11-digit product format
- 712750001
- Labeler code
- 71275
- Product ID
- 71275-001_9cbe75fe-457d-5654-e053-2995a90a3de4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium fluoride
- Dosage form
- PASTE, DENTIFRICE
- Route
- DENTAL
- Labeler
- BURST.USA.Inc
- Application
- part355
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2017-02-20
- Marketing end
- 0000-00-00
- Substance
- SODIUM FLUORIDE
- Active strength
- 0 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 71275-001-47 | BURSTWonderfully Whitening Anti Cavity | 133 g in 1 TUBE | PASTE, DENTIFRICE | 133 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71275-001 | BURST WONDERFULLY WHITENING ANTI CAVITY (SODIUM FLUORIDE) PASTE, DENTIFRICE [BURST.USA.INC] | 4 | Legacy NDC, 1 package rows | 20200124_48c22ca2-1238-6d6e-e054-00144ff8d46c.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 |
|---|
| 71275-001-47 | 71275000147 | 133 g in 1 TUBE (71275-001-47) | 133 g | 2017-02-20 | 0000-00-00 | No | No | Current |