Supersmile
- Product NDC
- 53567-0031
- 11-digit product format
- 535670031
- Labeler code
- 53567
- Product ID
- 53567-0031_47e56e2b-2f9d-1886-e063-6394a90af31f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Monofluorophosphate
- Dosage form
- PASTE, DENTIFRICE
- Route
- DENTAL
- Labeler
- Robell Research, Inc
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-10-15
- Substance
- SODIUM MONOFLUOROPHOSPHATE
- Active strength
- .14 g/100g
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Supersmile
- Brand name suffix
- Professional Whitening TP
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM MONOFLUOROPHOSPHATE | .14 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | C810JCZ56Q |
| Rxcui | 2695772 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 53567-0031-1 | SupersmileProfessional Whitening TP | 119 g in 1 TUBE | PASTE, DENTIFRICE | 119 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53567-0031 | SUPERSMILE PROFESSIONAL WHITENING TP (SODIUM MONOFLUOROPHOSPHATE) PASTE, DENTIFRICE [ROBELL RESEARCH, INC] | 2 | Current NDC, 1 package rows | 20250119_25021787-44e8-0b29-e063-6394a90a0af6.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 53567-0031-1 | 53567003101 | 119 g in 1 TUBE (53567-0031-1) | 119 g | 2024-10-15 | No | No | Current |