Anticavity Rinse
- Product NDC
- 37808-808
- 11-digit product format
- 378080808
- Labeler code
- 37808
- Product ID
- 37808-808_4b939a30-7110-d9b7-e063-6294a90a78ed
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Fluoride
- Dosage form
- MOUTHWASH
- Route
- ORAL
- Labeler
- H E B
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2010-02-25
- 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 |
|---|
| 37808-808-44 | Anticavity Rinse | 532 mL in 1 BOTTLE, PLASTIC | MOUTHWASH | 532 | | 13 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 37808-808 | ANTICAVITY RINSE (SODIUM FLUORIDE) MOUTHWASH [H-E-B] | 12 | Current NDC, Legacy NDC, 1 package rows | 20250322_51ddc81b-1c90-4998-b538-6761ac113437.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 |
|---|
| 37808-808-44 | 37808080844 | 532 mL in 1 BOTTLE, PLASTIC (37808-808-44) | 532 ml | 2010-02-25 | 0000-00-00 | No | No | Current |