PreviDent Alcohol Free
- Product NDC
- 0126-0033
- 11-digit product format
- 001260033
- Labeler code
- 0126
- Product ID
- 0126-0033_228280d8-dad7-4a08-98f4-e9166df917e8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium Fluoride
- Dosage form
- MOUTHWASH
- Route
- DENTAL
- Labeler
- Colgate Oral Pharmaceuticals, Inc.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2016-06-13
- Substance
- SODIUM FLUORIDE
- Active strength
- .9 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 Alcohol Free
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM FLUORIDE | .9 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 8ZYQ1474W7 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0126-0033-16 | PreviDent Alcohol Free | 473 mL in 1 BOTTLE, PLASTIC | MOUTHWASH | 473 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0126-0033 | PREVIDENT ALCOHOL FREE (SODIUM FLUORIDE) MOUTHWASH [COLGATE ORAL PHARMACEUTICALS, INC.] | 5 | Current NDC, Legacy NDC, 1 package rows | 20220713_28e4f7cd-9fd8-4c7a-9e4b-d747fefc76c0.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0126-0033-16 | 00126003316 | 473 mL in 1 BOTTLE, PLASTIC (0126-0033-16) | 473 ml | 2016-06-13 | 0000-00-00 | No | No | Current |