Anticavity Rinse
- Product NDC
- 11822-4004
- 11-digit product format
- 118224004
- Labeler code
- 11822
- Product ID
- 11822-4004_499ea74c-77d5-d1f8-e063-6294a90a8a72
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Fluoride
- Dosage form
- MOUTHWASH
- Route
- ORAL
- Labeler
- Rite Aid Corporation
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2022-12-05
- Substance
- SODIUM FLUORIDE
- Active strength
- .5 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 | .5 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 |
|---|
| 11822-4004-4 | Anticavity Rinse | 532 mL in 1 PACKAGE | MOUTHWASH | 532 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 11822-4004 | ANTICAVITY RINSE (SODIUM FLUORIDE) MOUTHWASH [RITE AID] | 3 | Current NDC, Legacy NDC, 1 package rows | 20240809_c1a22692-b955-498a-a7c1-1cd7bfd54bda.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 |
|---|
| 11822-4004-4 | 11822400404 | 532 mL in 1 PACKAGE (11822-4004-4) | 532 ml | 2022-12-05 | 0000-00-00 | No | No | Current |