PreviDent 5000 Booster Plus Spearmint
- Product NDC
- 0126-0074
- 11-digit product format
- 001260074
- Labeler code
- 0126
- Product ID
- 0126-0074_72a745ee-4ddb-4194-9f0a-54e20b566b0c
- 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 Spearmint
- 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 |
|---|
| 0126-0074-92 | PreviDent 5000 Booster Plus Spearmint | 100 mL in 1 BOTTLE, PLASTIC | PASTE, DENTIFRICE | 100 | | 10 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0126-0074 | PREVIDENT 5000 BOOSTER PLUS SPEARMINT (SODIUM FLUORIDE) PASTE, DENTIFRICE [COLGATE ORAL PHARMACEUTICALS, INC.] | 10 | Current NDC, Legacy NDC, 1 package rows | 20240316_4ef2b7ed-41c3-41cb-8ee0-1930ab8fb198.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 |
|---|
| 0126-0074-92 | 00126007492 | 100 mL in 1 BOTTLE, PLASTIC (0126-0074-92) | 100 ml | 2015-03-01 | 0000-00-00 | No | No | Current |