Super Vanilla Fluoride Mouthwash
- Product NDC
- 83729-104
- 11-digit product format
- 837290104
- Labeler code
- 83729
- Product ID
- 83729-104_e8a98e66-04c2-4c28-a355-09f5ff599bd6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Anticavity Mouthwash
- Dosage form
- LIQUID
- Route
- DENTAL
- Labeler
- SuperMouth, LLC.
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-03-21
- Substance
- SODIUM FLUORIDE
- Active strength
- .002 mg/10mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Super Vanilla Fluoride Mouthwash
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM FLUORIDE | .002 mg/10mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 8ZYQ1474W7 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 83729-104-16 | Super Vanilla Fluoride Mouthwash | 473 mL in 1 BOTTLE | LIQUID | 473 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 83729-104 | SUPER VANILLA FLUORIDE MOUTHWASH (ANTICAVITY MOUTHWASH) LIQUID [SUPERMOUTH, LLC.] | 1 | Current NDC, 1 package rows | 20250226_8c66e423-9f9a-46d6-a04f-feff34dc06c5.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 83729-104-16 | 83729010416 | 473 mL in 1 BOTTLE (83729-104-16) | 473 ml | 2023-03-21 | No | No | Current |