Alcohol-Free Anticavity
- Product NDC
- 36800-482
- 11-digit product format
- 368000482
- Labeler code
- 36800
- Product ID
- 36800-482_4ab9671f-9d7c-0b2a-e063-6294a90a50d0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium fluoride
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Topco Associates LLC
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2013-09-19
- 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
- Alcohol-Free 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 |
|---|
| 36800-482-86 | Alcohol-Free Anticavity | 1000 mL in 1 BOTTLE, PLASTIC | LIQUID | 1000 | | 21 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 36800-482 | ALCOHOL-FREE ANTICAVITY (SODIUM FLUORIDE) LIQUID [TOPCO ASSOCIATES LLC] | 19 | Current NDC, Legacy NDC, 1 package rows | 20240919_ade7dcb2-b4e2-4cef-b9a7-469867ead68a.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 |
|---|
| 36800-482-86 | 36800048286 | 1000 mL in 1 BOTTLE, PLASTIC (36800-482-86) | 1000 ml | 2013-09-19 | 0000-00-00 | No | No | Current |