Anticavity Fluoride Rinse
- Product NDC
- 36800-004
- 11-digit product format
- 368000004
- Labeler code
- 36800
- Product ID
- 36800-004_4ab75798-a4e5-d8f0-e063-6294a90ad09a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SODIUM FLUORIDE
- Dosage form
- RINSE
- Route
- ORAL
- Labeler
- Topco Associates LLC
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2004-04-08
- 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 Fluoride 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 |
|---|
| 36800-004-44 | Anticavity Fluoride Rinse | 532 mL in 1 BOTTLE, PLASTIC | RINSE | 532 | | 23 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 36800-004 | ANTICAVITY FLUORIDE RINSE (SODIUM FLUORIDE) RINSE [TOPCO ASSOCIATES LLC] | 22 | Current NDC, Legacy NDC, 1 package rows | 20250316_3b04142a-4a65-45ba-a5a2-e62b0c47ec55.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 |
|---|
| 36800-004-44 | 36800000444 | 532 mL in 1 BOTTLE, PLASTIC (36800-004-44) | 532 ml | 2004-04-08 | 0000-00-00 | No | No | Current |