PCXX ONE MINTE GEL CREME DE MENTHE
- Product NDC
- 62007-006
- 11-digit product format
- 620070006
- Labeler code
- 62007
- Product ID
- 62007-006_b2a2cf43-894c-4684-8389-b643e7e6cc84
- 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
- 27 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 |
|---|
| 62007-006-16 | PCXX ONE MINTE GEL CREME DE MENTHE | 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 |
|---|
| 62007-006 | PCXX ONE MINTE GEL CREME DE MENTHE (FLUORIDE TREATMENT) GEL [ROSS HEALTHCARE INC.] | 1 | Legacy NDC, 1 package rows | 20140530_47d28652-9ec2-4ca9-b6c7-8007b3e0963b.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 62007-006-16 | 62007000616 | 1 mg in 1 BOTTLE, PLASTIC | 1 mg | Historical |