Anticavity
- Product NDC
- 72288-439
- 11-digit product format
- 722880439
- Labeler code
- 72288
- Product ID
- 72288-439_4c20bcef-5513-c447-e063-6294a90a701b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium fluoride
- Dosage form
- MOUTHWASH
- Route
- ORAL
- Labeler
- Amazon.com Services LLC
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2018-05-01
- 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 |
|---|
| 72288-439-43 | Anticavity | 473 mL in 1 BOTTLE, PLASTIC | MOUTHWASH | 473 | | 15 |
| 72288-439-45 | Anticavity | 946 mL in 1 BOTTLE, PLASTIC | MOUTHWASH | 946 | | 15 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72288-439 | ANTICAVITY (SODIUM FLUORIDE) MOUTHWASH [AMAZON.COM SERVICES LLC] | 13 | Current NDC, Legacy NDC, 2 package rows | 20250221_4a0220f8-748f-4a4a-9a8b-948756468f82.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 |
|---|
| 72288-439-43 | 72288043943 | 473 mL in 1 BOTTLE, PLASTIC (72288-439-43) | 473 ml | 2018-05-01 | 0000-00-00 | No | No | Current |
| 72288-439-45 | 72288043945 | 946 mL in 1 BOTTLE, PLASTIC (72288-439-45) | 946 ml | 2018-05-01 | 0000-00-00 | No | No | Current |