Anticavity Fluoride Rinse
- Product NDC
- 72036-213
- 11-digit product format
- 720360213
- Labeler code
- 72036
- Product ID
- 72036-213_4a043690-9d27-33ba-e063-6394a90aa04e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Fluoride
- Dosage form
- MOUTHWASH
- Route
- ORAL
- Labeler
- HARRIS TEETER
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2009-05-14
- 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 Fluoride Rinse
- 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 |
|---|
| 72036-213-44 | Anticavity Fluoride Rinse | 532 mL in 1 BOTTLE, PLASTIC | MOUTHWASH | 532 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72036-213 | ANTICAVITY FLUORIDE RINSE (SODIUM FLUORIDE) MOUTHWASH [HARRIS TEETER, LLC] | 3 | Current NDC, 1 package rows | 20250503_f759e9e4-6de2-4b80-903b-e67c06e36295.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72036-213-44 | 72036021344 | 532 mL in 1 BOTTLE, PLASTIC (72036-213-44) | 532 ml | 2009-05-14 | No | No | Current |