Zap APF
- Product NDC
- 24794-103
- 11-digit product format
- 247940103
- Labeler code
- 24794
- Product ID
- 24794-103_d61895e1-6f77-4d3d-e053-2995a90a1729
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium Fluoride
- Dosage form
- GEL
- Route
- DENTAL
- Labeler
- Crosstex International Inc.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2012-12-14
- 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
- Zap 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 |
|---|
| 24794-103-16 | Zap APF | 454 g in 1 BOTTLE, PLASTIC | GEL | 454 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 24794-103 | ZAP APF (SODIUM FLUORIDE) GEL [CROSSTEX INTERNATIONAL INC.] | 5 | Current NDC, Legacy NDC, 1 package rows | 20220122_ec50b003-cf61-4f66-bb62-f779e48363c2.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 |
|---|
| 24794-103-16 | 24794010316 | 454 g in 1 BOTTLE, PLASTIC (24794-103-16) | 454 g | 2018-06-01 | 0000-00-00 | No | No | Current |