ADVANCED WHITENING ANTI CAVITY FLUORIDE
- Product NDC
- 52000-108
- 11-digit product format
- 520000108
- Labeler code
- 52000
- Product ID
- 52000-108_ede5654c-864e-44c6-904b-ca2ac4532096
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Monofluorophosphate
- Dosage form
- PASTE
- Route
- DENTAL
- Labeler
- Universal Distribution Center LLC
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-05-18
- Substance
- SODIUM MONOFLUOROPHOSPHATE
- Active strength
- .76 g/100g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- ADVANCED WHITENING ANTI CAVITY FLUORIDE
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM MONOFLUOROPHOSPHATE | .76 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | C810JCZ56Q |
| Rxcui | 545626 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 52000-108-01 | ADVANCED WHITENING ANTI CAVITY FLUORIDE | 181 g in 1 TUBE | PASTE | 181 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 52000-108 | ADVANCED WHITENING ANTI CAVITY FLUORIDE (SODIUM MONOFLUOROPHOSPHATE) PASTE [UNIVERSAL DISTRIBUTION CENTER LLC] | 2 | Current NDC, Legacy NDC, 1 package rows | 20231121_8ea8a8d9-b7e4-468f-9a09-4ec634cbd80e.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 52000-108-01 | 52000010801 | 181 g in 1 TUBE (52000-108-01) | 181 g | 2020-05-18 | 0000-00-00 | No | No | Current |