Enamur Fluoride AntiCavity Toothpast
- Product NDC
- 83610-1050
- 11-digit product format
- 836101050
- Labeler code
- 83610
- Product ID
- 83610-1050_39962a9d-e97a-d260-e063-6394a90a1b40
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Fluoride Toothpast
- Dosage form
- PASTE, DENTIFRICE
- Route
- ORAL
- Labeler
- Protegera, Inc
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-06-30
- Substance
- SODIUM FLUORIDE
- Active strength
- 1.4 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
- Enamur Fluoride AntiCavity Toothpast
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM FLUORIDE | 1.4 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 8ZYQ1474W7 |
| Rxcui | 416783 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 83610-1050-1 | Enamur Fluoride AntiCavity Toothpast | 1 in 1 CARTON | PASTE, DENTIFRICE | 1 | | 4 |
| 83610-1050-1 | Enamur Fluoride AntiCavity Toothpast | 147 g in 1 TUBE | PASTE, DENTIFRICE | 147 | | 4 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 83610-1050-1 | 83610105001 | 1 TUBE in 1 CARTON (83610-1050-1) / 147 g in 1 TUBE | 1 tube | 2025-06-30 | No | No | Historical |