PCXX REMIN 0.4
- Product NDC
- 62007-041
- 11-digit product format
- 620070041
- Labeler code
- 62007
- Product ID
- 62007-041_83d5b60e-f021-4617-e053-2a91aa0a7537
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- SODIUM FLUORIDE
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Ross Healthcare Inc.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2015-02-16
- Marketing end
- 0000-00-00
- Substance
- SODIUM FLUORIDE
- Active strength
- 20 mg/mg
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 62007-041-02 | PCXX REMIN 0.4 | 1 mg in 1 BOTTLE, PLASTIC | GEL | 1 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 62007-041 | PCXX REMIN 0.4 (SODIUM FLUORIDE) GEL [ROSS HEALTHCARE INC.] | 2 | Legacy NDC, 1 package rows | 20190312_5d489e8b-58a0-4d4a-940e-e6906256c573.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 62007-041-02 | 62007004102 | 1 mg in 1 BOTTLE, PLASTIC | 1 mg | Historical |