TARGET UP AND UP ANTICAVITY
- Product NDC
- 82442-106
- 11-digit product format
- 824420106
- Labeler code
- 82442
- Product ID
- 82442-106_40ab0ae2-4f73-e0d4-e063-6394a90a9b43
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SODIUM FLUORIDE 0.05%
- Dosage form
- MOUTHWASH
- Route
- ORAL
- Labeler
- TARGET CORPORATION
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-12-18
- Substance
- SODIUM FLUORIDE
- Active strength
- .05 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- TARGET UP AND UP ANTICAVITY
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM FLUORIDE | .05 g/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 8ZYQ1474W7 |
| Rxcui | 240698 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 82442-106-16 | TARGET UP AND UP ANTICAVITY | 473 mL in 1 BOTTLE | MOUTHWASH | 473 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 82442-106 | TARGET UP AND UP ANTICAVITY (SODIUM FLUORIDE 0.05%) MOUTHWASH [TARGET CORPORATION] | 1 | Current NDC, 1 package rows | 20241220_2992efce-1c66-df40-e063-6294a90ab3c0.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 |
|---|
| 82442-106-16 | 82442010616 | 473 mL in 1 BOTTLE (82442-106-16) | 473 ml | 2024-12-18 | No | No | Current |