Anticavity
- Product NDC
- 49035-581
- 11-digit product format
- 490350581
- Labeler code
- 49035
- Product ID
- 49035-581_4bd50069-b71a-f46e-e063-6294a90a93f9
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium fluoride
- Dosage form
- MOUTHWASH
- Route
- ORAL
- Labeler
- Walmart Inc.
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2016-09-25
- 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
- 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 | 313029 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 49035-581-86 | Anticavity | 1000 mL in 1 BOTTLE, PLASTIC | MOUTHWASH | 1000 | | 16 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 49035-581 | ANTICAVITY (SODIUM FLUORIDE) MOUTHWASH [WAL-MART STORES, INC] | 14 | Current NDC, Legacy NDC, 1 package rows | 20240730_af5b93e7-5cce-4e01-8df2-54494d8b2910.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 |
|---|
| 49035-581-86 | 49035058186 | 1000 mL in 1 BOTTLE, PLASTIC (49035-581-86) | 1000 ml | 2016-09-25 | 0000-00-00 | No | No | Current |