Auraglow Whitening
- Product NDC
- 81740-003
- 11-digit product format
- 817400003
- Labeler code
- 81740
- Product ID
- 81740-003_3f72b20e-32ad-468c-a67b-ff438c3a8396
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SODIUM FLUORIDE
- Dosage form
- PASTE, DENTIFRICE
- Route
- DENTAL
- Labeler
- Auraglow LLC
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-10-20
- Substance
- SODIUM FLUORIDE
- Active strength
- 2.3 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
- Auraglow Whitening
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM FLUORIDE | 2.3 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 8ZYQ1474W7 |
| Rxcui | 1489127 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 81740-003-03 | Auraglow Whitening | 1 in 1 CARTON | PASTE, DENTIFRICE | 1 | | 1 |
| 81740-003-03 | Auraglow Whitening | 113 g in 1 TUBE | PASTE, DENTIFRICE | 113 | | 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 |
|---|
| 81740-003-03 | 81740000303 | 1 TUBE in 1 CARTON (81740-003-03) / 113 g in 1 TUBE | 1 tube | 2025-10-20 | No | No | Historical |