Anticavity
- Product NDC
- 41163-011
- 11-digit product format
- 411630011
- Labeler code
- 41163
- Product ID
- 41163-011_4b088b88-cd28-9a1c-e063-6394a90a67d6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium fluoride
- Dosage form
- MOUTHWASH
- Route
- ORAL
- Labeler
- United Natural Foods, Inc. dba UNFI
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2015-12-18
- Substance
- SODIUM FLUORIDE
- Active strength
- .1 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 | .1 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 8ZYQ1474W7 |
| Rxcui | 313029 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 41163-011-45 | Anticavity | 946 mL in 1 BOTTLE, PLASTIC | MOUTHWASH | 946 | | 17 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 41163-011 | ANTICAVITY (SODIUM FLUORIDE) MOUTHWASH [UNITED NATURAL FOODS, INC. DBA UNFI] | 16 | Current NDC, Legacy NDC, 1 package rows | 20250417_dd6bf8df-1e28-4f61-b876-b9f1f8d5993a.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 |
|---|
| 41163-011-45 | 41163001145 | 946 mL in 1 BOTTLE, PLASTIC (41163-011-45) | 946 ml | 2015-12-18 | 0000-00-00 | No | No | Current |