Anticavity fluoride rinse
- Product NDC
- 79481-0838
- 11-digit product format
- 794810838
- Labeler code
- 79481
- Product ID
- 79481-0838_4b3480bd-bd55-1325-e063-6394a90ad76c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium fluoride
- Dosage form
- MOUTHWASH
- Route
- ORAL
- Labeler
- Meijer, Inc.
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-09-29
- Substance
- SODIUM FLUORIDE
- Active strength
- .2 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Anticavity fluoride rinse
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM FLUORIDE | .2 mg/mL |
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 |
|---|
| 79481-0838-1 | Anticavity fluoride rinse | 296 mL in 1 BOTTLE, PLASTIC | MOUTHWASH | 296 | | 3 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 79481-0838-1 | 79481083801 | 296 mL in 1 BOTTLE, PLASTIC (79481-0838-1) | 296 ml | 2025-09-29 | No | No | Current |