Super Vanilla
- Product NDC
- 83729-115
- 11-digit product format
- 837290115
- Labeler code
- 83729
- Product ID
- 83729-115_ae428dfe-5a09-4024-ba0a-e88e8b7c6c11
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Vanilla Toothpaste
- Dosage form
- PASTE, DENTIFRICE
- Route
- DENTAL
- Labeler
- SuperMouth, LLC.
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-06-30
- Substance
- SODIUM FLUORIDE
- Active strength
- 2.4 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
- Super Vanilla
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM FLUORIDE | 2.4 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 |
|---|
| 83729-115-10 | Super Vanilla | 1 in 1 CARTON | PASTE, DENTIFRICE | 1 | | 1 |
| 83729-115-10 | Super Vanilla | 96 g in 1 TUBE | PASTE, DENTIFRICE | 96 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 83729-115-10 | 83729011510 | 1 in 1 CARTON | Historical |