ANTICAVITY FLUORIDE
- Product NDC
- 73928-090
- 11-digit product format
- 739280090
- Labeler code
- 73928
- Product ID
- 73928-090_45af957c-052e-c7b0-e063-6394a90a34fd
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SODIUM FLUORIDE
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Kingkey MBC Life Technology Group co., LTD
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-12-01
- Substance
- SODIUM FLUORIDE
- Active strength
- .05 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- ANTICAVITY FLUORIDE
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM FLUORIDE | .05 g/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 8ZYQ1474W7 |
| Rxcui | 2682817 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 73928-090-01 | ANTICAVITY FLUORIDE | 355 mL in 1 BOTTLE | LIQUID | 355 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 73928-090 | ANTICAVITY FLUORIDE (SODIUM FLUORIDE) LIQUID [KINGKEY MBC LIFE TECHNOLOGY GROUP CO., LTD] | 1 | Current NDC, 1 package rows | 20241219_295b88e8-c4b5-c0b0-e063-6394a90aca01.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 |
|---|
| 73928-090-01 | 73928009001 | 355 mL in 1 BOTTLE (73928-090-01) | 355 ml | 2024-12-01 | No | No | Current |