PreviDent 5000 Booster Plus Fruitastic
- Product NDC
- 0126-0072
- 11-digit product format
- 001260072
- Labeler code
- 0126
- Product ID
- 0126-0072_64ffd747-d139-4f43-8dbb-a04ac332b620
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium Fluoride
- Dosage form
- PASTE, DENTIFRICE
- Route
- DENTAL
- Labeler
- Colgate Oral Pharmaceuticals, Inc.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2015-03-01
- Substance
- SODIUM FLUORIDE
- Active strength
- 6 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- PreviDent 5000 Booster Plus Fruitastic
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM FLUORIDE | 6 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 8ZYQ1474W7 |
| Rxcui | 392038, 630194 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0126-0072-92 | PreviDent 5000 Booster Plus Fruitastic | 100 mL in 1 BOTTLE, PLASTIC | PASTE, DENTIFRICE | 100 | | 12 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0126-0072 | PREVIDENT 5000 BOOSTER PLUS FRUITASTIC (SODIUM FLUORIDE) PASTE, DENTIFRICE [COLGATE ORAL PHARMACEUTICALS, INC.] | 11 | Current NDC, Legacy NDC, 1 package rows | 20230603_83986c58-25ed-45a4-9d19-36f6ce32d76c.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 |
|---|
| 0126-0072-92 | 00126007292 | 100 mL in 1 BOTTLE, PLASTIC (0126-0072-92) | 100 ml | 2015-03-01 | 0000-00-00 | No | No | Current |