dentalux ANTI-CAVITY FLUORIDE
- Product NDC
- 71141-186
- 11-digit product format
- 711410186
- Labeler code
- 71141
- Product ID
- 71141-186_77de6540-40df-4421-9242-a418ba5c2074
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Monofluorophosphate
- Dosage form
- PASTE, DENTIFRICE
- Route
- DENTAL
- Labeler
- Lidl US, LLC
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-06-30
- Substance
- SODIUM MONOFLUOROPHOSPHATE
- Active strength
- .13 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
- dentalux ANTI-CAVITY FLUORIDE
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM MONOFLUOROPHOSPHATE | .13 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 |
|---|
| 71141-186-10 | dentalux ANTI-CAVITY FLUORIDE | 1 in 1 BOX | PASTE, DENTIFRICE | 1 | | 1 |
| 71141-186-10 | dentalux ANTI-CAVITY FLUORIDE | 113 g in 1 TUBE | PASTE, DENTIFRICE | 113 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71141-186 | DENTALUX ANTI-CAVITY FLUORIDE (SODIUM MONOFLUOROPHOSPHATE) PASTE, DENTIFRICE [LIDL US, LLC] | 1 | Current NDC, 2 package rows | 20241121_ccf54743-81c2-43f8-9c5c-d4baa85fc18d.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 |
|---|
| 71141-186-10 | 71141018610 | 1 TUBE in 1 BOX (71141-186-10) / 113 g in 1 TUBE | 1 tube | 2024-06-30 | No | No | Historical |