PureLife APF
- Product NDC
- 68987-012
- 11-digit product format
- 689870012
- Labeler code
- 68987
- Product ID
- 68987-012_d5f3e776-11ac-7413-e053-2995a90a4603
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium Fluoride
- Dosage form
- GEL
- Route
- DENTAL
- Labeler
- PureLife Dental
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2012-12-18
- Substance
- SODIUM FLUORIDE
- Active strength
- 5.6 g/454g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- PureLife APF
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM FLUORIDE | 5.6 g/454g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 8ZYQ1474W7 |
| Rxcui | 245593 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68987-012-15 | PureLife APF | 454 g in 1 BOTTLE, PLASTIC | GEL | 454 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68987-012 | PURELIFE APF (SODIUM FLUORIDE) GEL [PURELIFE DENTAL] | 4 | Current NDC, Legacy NDC, 1 package rows | 20220120_615840e4-c108-4d68-b815-fc95ae75539c.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 |
|---|
| 68987-012-15 | 68987001215 | 454 g in 1 BOTTLE, PLASTIC (68987-012-15) | 454 g | 2016-07-01 | 0000-00-00 | No | No | Current |