Anticavity
- Product NDC
- 69842-548
- 11-digit product format
- 698420548
- Labeler code
- 69842
- Product ID
- 69842-548_4b7e91d9-fa8a-2d76-e063-6294a90a71eb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Fluoride
- Dosage form
- RINSE
- Route
- ORAL
- Labeler
- CVS Pharmacy, Inc.
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2021-04-20
- 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 |
|---|
| 69842-548-86 | Anticavity | 1000 mL in 1 BOTTLE, PLASTIC | RINSE | 1000 | | 14 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69842-548 | ANTICAVITY (SODIUM FLUORIDE) RINSE [CVS PHARMACY, INC] | 12 | Current NDC, Legacy NDC, 1 package rows | 20250302_344c9d00-ad82-46a9-83e9-68197e1a68bb.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 |
|---|
| 69842-548-86 | 69842054886 | 1000 mL in 1 BOTTLE, PLASTIC (69842-548-86) | 1000 ml | 2021-04-20 | 0000-00-00 | No | No | Current |