Anticavity Rinse
- Product NDC
- 49035-004
- 11-digit product format
- 490350004
- Labeler code
- 49035
- Product ID
- 49035-004_4bd29ab1-6fdb-5cb4-e063-6294a90a9bdd
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Fluoride
- Dosage form
- MOUTHWASH
- Route
- ORAL
- Labeler
- Walmart Inc.
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2004-04-06
- Substance
- SODIUM FLUORIDE
- Active strength
- .2 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 Rinse
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM FLUORIDE | .2 mg/mL |
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 |
|---|
| 49035-004-44 | Anticavity Rinse | 532 mL in 1 BOTTLE, PLASTIC | MOUTHWASH | 532 | | 23 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 49035-004 | ANTICAVITY RINSE (SODIUM FLUORIDE) MOUTHWASH [WAL MART] | 22 | Current NDC, Legacy NDC, 1 package rows | 20250426_3beb65e4-ae8e-4e51-b9ba-181cbec41eff.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 |
|---|
| 49035-004-44 | 49035000444 | 532 mL in 1 BOTTLE, PLASTIC (49035-004-44) | 532 ml | 2004-04-06 | 0000-00-00 | No | No | Current |