PCXX ROOTBEER APF F
- Product NDC
- 62007-060
- 11-digit product format
- 620070060
- Labeler code
- 62007
- Product ID
- 62007-060_5e8680eb-43c1-7403-e053-2a91aa0adcec
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium Fluoride
- Dosage form
- AEROSOL, FOAM
- Route
- DENTAL; TOPICAL
- Labeler
- Ross Healthcare Inc.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2017-11-21
- Marketing end
- 0000-00-00
- Substance
- SODIUM FLUORIDE
- Active strength
- 0 g/g
- 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 |
|---|
| 62007-060-07 | PCXX ROOTBEER APF F | 125 g in 1 CAN | AEROSOL, FOAM | 125 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 62007-060 | PCXX ROOTBEER APF F (SODIUM FLUORIDE) AEROSOL, FOAM [ROSS HEALTHCARE INC.] | 1 | Legacy NDC, 1 package rows | 20171122_5e8659ca-f158-0270-e053-2991aa0afefc.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 62007-060-07 | 62007006007 | 125 g in 1 CAN | 125 g | Historical |