Vortex
- Product NDC
- 52316-028
- 11-digit product format
- 523160028
- Labeler code
- 52316
- Product ID
- 52316-028_8ecf77c1-f102-4992-a08e-6f3d42a6036b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Toothpaste
- Dosage form
- PASTE, DENTIFRICE
- Route
- DENTAL
- Labeler
- DSC Laboratories, Div. of DSC Products Inc.
- Application
- part355
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2011-12-30
- Marketing end
- 0000-00-00
- Substance
- SODIUM FLUORIDE
- Active strength
- 2 mg/g
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- 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 |
|---|
| 52316-028-42 | Vortex | 120 g in 1 TUBE | PASTE, DENTIFRICE | 120 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 52316-028 | VORTEX (TOOTHPASTE) PASTE, DENTIFRICE [DSC LABORATORIES, DIV. OF DSC PRODUCTS INC.] | 1 | Legacy NDC, 1 package rows | 20111230_47aef72b-2f09-4d08-b2d2-01b32e9e9faf.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 52316-028-42 | 52316002842 | 120 g in 1 TUBE | 120 g | Historical |