UNIVERSAL ANTI-CAVITY FLUORIDE
- Product NDC
- 52000-111
- 11-digit product format
- 520000111
- Labeler code
- 52000
- Product ID
- 52000-111_42b18d2a-c986-42a0-9f88-9ee8e8b1290b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Monofluorophosphate
- Dosage form
- PASTE
- Route
- DENTAL
- Labeler
- Universal Distribution Center LLC
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-05-30
- Substance
- SODIUM MONOFLUOROPHOSPHATE
- Active strength
- .76 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 ANTI-CAVITY FLUORIDE
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM MONOFLUOROPHOSPHATE | .76 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | C810JCZ56Q |
| Rxcui | 545626 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 52000-111-01 | UNIVERSAL ANTI-CAVITY FLUORIDE | 181 g in 1 TUBE | PASTE | 181 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 52000-111 | UNIVERSAL ANTI-CAVITY FLUORIDE (SODIUM MONOFLUOROPHOSPHATE) PASTE [UNIVERSAL DISTRIBUTION CENTER LLC] | 2 | Current NDC, Legacy NDC, 1 package rows | 20231121_e3356374-befa-41b0-ab0f-edfd5a062601.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 |
|---|
| 52000-111-01 | 52000011101 | 181 g in 1 TUBE (52000-111-01) | 181 g | 2020-05-30 | 0000-00-00 | No | No | Current |