Anticavity Fluoride Rinse
- Product NDC
- 11673-163
- 11-digit product format
- 116730163
- Labeler code
- 11673
- Product ID
- 11673-163_4b1e3881-571e-9711-e063-6294a90a2f94
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SODIUM FLUORIDE
- Dosage form
- MOUTHWASH
- Route
- ORAL
- Labeler
- Target Corporation
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 1994-04-06
- 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 Fluoride Rinse
- 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#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 11673-163-86 | Anticavity Fluoride Rinse | 1000 mL in 1 BOTTLE, PLASTIC | MOUTHWASH | 1000 | | 19 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 11673-163 | ANTICAVITY FLUORIDE RINSE (SODIUM FLUORIDE) MOUTHWASH [TARGET CORPORATION] | 17 | Current NDC, Legacy NDC, 1 package rows | 20241215_3e4119b2-9506-4305-8cff-163f700265d0.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 |
|---|
| 11673-163-86 | 11673016386 | 1000 mL in 1 BOTTLE, PLASTIC (11673-163-86) | 1000 ml | 1994-04-06 | 0000-00-00 | No | No | Current |