Anticavity Fluoride Rinse
- Product NDC
- 71141-159
- 11-digit product format
- 711410159
- Labeler code
- 71141
- Product ID
- 71141-159_4a052a47-2017-3a0f-e063-6294a90aaf54
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Fluoride
- Dosage form
- MOUTHWASH
- Route
- ORAL
- Labeler
- Lidl US, LLC
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2017-02-09
- Substance
- SODIUM FLUORIDE
- Active strength
- .1 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Anticavity Fluoride Rinse
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM FLUORIDE | .1 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 8ZYQ1474W7 |
| Rxcui | 313029 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71141-159-32 | Anticavity Fluoride Rinse | 1000 mL in 1 PACKAGE | MOUTHWASH | 1000 | | 15 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71141-159 | ANTICAVITY FLUORIDE RINSE (SODIUM FLUORIDE) MOUTHWASH [LIDL US, LLC] | 14 | Current NDC, Legacy NDC, 1 package rows | 20250328_c47475aa-3125-410f-aa31-0add6e4ce125.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 |
|---|
| 71141-159-32 | 71141015932 | 1000 mL in 1 PACKAGE (71141-159-32) | 1000 ml | 2017-02-09 | 0000-00-00 | No | No | Current |