evo SENSITIVE WHITENING ANTI-CAVITY FLUORIDE
- Product NDC
- 70108-210
- 11-digit product format
- 701080210
- Labeler code
- 70108
- Product ID
- 70108-210_cdc9d79b-c80c-443e-9c18-71dfd970cc76
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Fluoride
- Dosage form
- MOUTHWASH
- Route
- ORAL
- Labeler
- Ashtel Studios, Inc.
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-07-10
- Substance
- SODIUM FLUORIDE
- Active strength
- .05 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- evo SENSITIVE WHITENING ANTI-CAVITY FLUORIDE
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM FLUORIDE | .05 g/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 8ZYQ1474W7 |
| Rxcui | 240698 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70108-210-01 | evo SENSITIVE WHITENING ANTI-CAVITY FLUORIDE | 296 mL in 1 BOTTLE | MOUTHWASH | 296 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70108-210-01 | 70108021001 | 296 mL in 1 BOTTLE (70108-210-01) | 296 ml | 2025-07-10 | No | No | Current |