PCXX CHERRY APF G
- Product NDC
- 62007-803
- 11-digit product format
- 620070803
- Labeler code
- 62007
- Product ID
- 62007-803_ba3dccee-b4d8-a919-e053-2a95a90a5a2f
- 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
- 2019-02-04
- Marketing end
- 0000-00-00
- Substance
- SODIUM FLUORIDE
- Active strength
- 27 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 62007-803 | PCXX CHERRY APF G (SODIUM FLUORIDE) GEL [ROSS HEALTHCARE INC.] | 5 | Legacy NDC | 20250201_8281515f-08b1-509c-e053-2a91aa0abae3.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 62007-803-16 | 62007080316 | 473 mL in 1 BOTTLE, PLASTIC (62007-803-16) | 473 ml | 2019-02-04 | 0000-00-00 | No | No | Current |