Dr.NOAH SOLIDTOOTHPASTE
- Product NDC
- 82359-0003
- 11-digit product format
- 823590003
- Labeler code
- 82359
- Product ID
- 82359-0003_cf7c2791-c3b5-2163-e053-2995a90a4e8e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- sodium fluoride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- DR.Noah
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2021-10-29
- Marketing end
- 0000-00-00
- Substance
- SODIUM FLUORIDE; SILICON DIOXIDE; SODIUM PYROPHOSPHATE; PYRIDOXINE HYDROCHLORIDE
- Active strength
- 0 g/1; g/1; g/1; g/1
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 82359-0003-1 | Dr.NOAH SOLIDTOOTHPASTE | 180 in 1 POUCH | TABLET | 180 | | 1 |
| 82359-0003-2 | Dr.NOAH SOLIDTOOTHPASTE | 30 in 1 CASE | TABLET | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 82359-0003 | DR.NOAH SOLIDTOOTHPASTE (SODIUM FLUORIDE) TABLET [DR.NOAH] | 1 | Legacy NDC, 2 package rows | 20211112_cf7c2791-c3b4-2163-e053-2995a90a4e8e.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 82359-0003-1 | 82359000301 | 180 TABLET in 1 POUCH (82359-0003-1) | 180 tablet | 2021-10-29 | 0000-00-00 | No | No | Current |
| 82359-0003-2 | 82359000302 | 30 TABLET in 1 CASE (82359-0003-2) | 30 tablet | 2021-10-29 | 0000-00-00 | No | No | Current |