PCXX WATERMELON APF G
- Product NDC
- 62007-813
- 11-digit product format
- 620070813
- Labeler code
- 62007
- Product ID
- 62007-813_4c11499d-25cf-e53a-e063-6394a90ad974
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium Fluoride
- Dosage form
- GEL
- Route
- DENTAL; TOPICAL
- Labeler
- Ross Healthcare Inc.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2019-02-22
- Substance
- SODIUM FLUORIDE
- Active strength
- 27.2 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- PCXX WATERMELON APF G
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM FLUORIDE | 27.2 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 8ZYQ1474W7 |
| Rxcui | 1535362 |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 62007-813-16 | PCXX WATERMELON APF G | 473 mL in 1 BOTTLE, PLASTIC | GEL | 473 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 62007-813 | PCXX WATERMELON APF G (SODIUM FLUORIDE) GEL [ROSS HEALTHCARE INC.] | 5 | Current NDC, Legacy NDC, 1 package rows | 20250201_8287b2de-028a-3eaa-e053-2a91aa0a0bd3.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 |
|---|
| 62007-813-16 | 62007081316 | 473 mL in 1 BOTTLE, PLASTIC (62007-813-16) | 473 ml | 2019-02-22 | 0000-00-00 | No | No | Current |