Spry Dentifrice
- Product NDC
- 27017-142
- 11-digit product format
- 270170142
- Labeler code
- 27017
- Product ID
- 27017-142_43567bbc-b07f-b605-e063-6294a90aad78
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Toothpaste
- Dosage form
- PASTE, DENTIFRICE
- Route
- ORAL
- Labeler
- Xlear Inc.
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2017-06-11
- Substance
- SODIUM FLUORIDE
- Active strength
- 2.43 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
- Spry Dentifrice
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM FLUORIDE | 2.43 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 8ZYQ1474W7 |
| Rxcui | 891775 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 27017-142-01 | Spry Dentifrice | 1 g in 1 TUBE | PASTE, DENTIFRICE | 1 | | 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 |
|---|
| 27017-142-01 | 27017014201 | 1 g in 1 TUBE (27017-142-01) | 1 g | 2017-06-11 | No | No | Current |