Anticavity
- Product NDC
- 11673-004
- 11-digit product format
- 116730004
- Labeler code
- 11673
- Product ID
- 11673-004_4b1dd4df-4c3d-c4fb-e063-6294a90a25e0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium fluoride
- Dosage form
- RINSE
- Route
- ORAL
- Labeler
- Target Corporation
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2011-08-26
- 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
- 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 |
|---|
| 11673-004-77 | Anticavity | 500 mL in 1 BOTTLE, PLASTIC | RINSE | 500 | | 19 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 11673-004 | ANTICAVITY (SODIUM FLUORIDE) RINSE [TARGET CORP] | 18 | Current NDC, Legacy NDC, 1 package rows | 20250322_abfc1973-60ab-44e5-8147-33739d8bd7a3.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 |
|---|
| 11673-004-77 | 11673000477 | 500 mL in 1 BOTTLE, PLASTIC (11673-004-77) | 500 ml | 2011-08-26 | 0000-00-00 | No | No | Current |