UNIVERSAL SENSITIVE ANTI-CAVITY FLUORIDE
- Product NDC
- 52000-109
- 11-digit product format
- 520000109
- Labeler code
- 52000
- Product ID
- 52000-109_1199f2f8-98e4-4b76-9be9-3b921495a3c3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- potassium nitrate and sodium fluoride
- Dosage form
- PASTE
- Route
- DENTAL
- Labeler
- Universal Distribution Center LLC
- Application
- M022
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-05-20
- Substance
- POTASSIUM NITRATE; SODIUM FLUORIDE
- Active strength
- 5; .15 g/100g; g/100g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- UNIVERSAL SENSITIVE ANTI-CAVITY FLUORIDE
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| POTASSIUM NITRATE | 5 g/100g |
| SODIUM FLUORIDE | .15 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | RU45X2JN0Z, 8ZYQ1474W7 |
| Rxcui | 1038841 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 52000-109-01 | UNIVERSAL SENSITIVE ANTI-CAVITY FLUORIDE | 122 g in 1 TUBE | PASTE | 122 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 52000-109 | UNIVERSAL SENSITIVE ANTI-CAVITY FLUORIDE (POTASSIUM NITRATE AND SODIUM FLUORIDE) PASTE [UNIVERSAL DISTRIBUTION CENTER LLC] | 2 | Current NDC, Legacy NDC, 1 package rows | 20231121_fcf59439-7e06-4129-a89f-cdeecdf8d488.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 |
|---|
| 52000-109-01 | 52000010901 | 122 g in 1 TUBE (52000-109-01) | 122 g | 2020-05-20 | 0000-00-00 | No | No | Current |