PCXX CREME DE MENTHE NEUTRAL GL
- Product NDC
- 62007-820
- 11-digit product format
- 620070820
- Labeler code
- 62007
- Product ID
- 62007-820_ba3dccee-b4d5-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
- 2019-02-22
- Marketing end
- 0000-00-00
- Substance
- SODIUM FLUORIDE
- Active strength
- 20 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 Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 62007-820-16 | PCXX CREME DE MENTHE NEUTRAL GL | 473 mL in 1 BOTTLE, PLASTIC | GEL | 473 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 62007-820 | PCXX CREME DE MENTHE NEUTRAL GL (SODIUM FLUORIDE) GEL [ROSS HEALTHCARE INC.] | 5 | Legacy NDC, 1 package rows | 20250201_8282caef-db9c-122b-e053-2a91aa0a8bdd.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 |
|---|
| 62007-820-16 | 62007082016 | 473 mL in 1 BOTTLE, PLASTIC (62007-820-16) | 473 ml | 2019-02-22 | 0000-00-00 | No | No | Current |