PCXX NEUTRAL GEL VANILLA ORANGE
- Product NDC
- 62007-023
- 11-digit product format
- 620070023
- Labeler code
- 62007
- Product ID
- 62007-023_5929cf3f-28ec-4528-b375-68e19357e926
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FLUORIDE TREATMENT
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Ross Healthcare Inc.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2014-05-21
- Marketing end
- 0000-00-00
- Substance
- SODIUM FLUORIDE
- Active strength
- 20 mg/mg
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 62007-023-16 | PCXX NEUTRAL GEL VANILLA ORANGE | 1 mg in 1 BOTTLE, PLASTIC | GEL | 1 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 62007-023 | PCXX NEUTRAL GEL VANILLA ORANGE (FLUORIDE TREATMENT) GEL [ROSS HEALTHCARE INC.] | 1 | Legacy NDC, 1 package rows | 20140530_edb1bf8e-21ee-442c-a81b-39c1684aea87.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 62007-023-16 | 62007002316 | 1 mg in 1 BOTTLE, PLASTIC | 1 mg | Historical |