Dentisse
- Product NDC
- 70683-0703
- 11-digit product format
- 706830703
- Labeler code
- 70683
- Product ID
- 70683-0703_42c83cbe-24d7-6ccb-e063-6294a90ab55b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Fluoride
- Dosage form
- PASTE, DENTIFRICE
- Route
- DENTAL; ORAL
- Labeler
- Dentisse, Inc.
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2014-02-13
- Substance
- SODIUM FLUORIDE
- Active strength
- 1.1 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Dentisse
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM FLUORIDE | 1.1 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 8ZYQ1474W7 |
| Rxcui | 891775 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70683-0703-2 | Dentisse | 91 g in 1 TUBE | PASTE, DENTIFRICE | 91 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70683-0703 | DENTISSE (SODIUM FLUORIDE) PASTE, DENTIFRICE [DENTISSE, INC.] | 2 | Current NDC, Legacy NDC, 1 package rows | 20231220_326b290a-9bd2-468e-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 |
|---|
| 70683-0703-2 | 70683070302 | 91 g in 1 TUBE (70683-0703-2) | 91 g | 2014-02-13 | 0000-00-00 | No | No | Current |