PCXX NEUTRAL FOAM BAZOOKA BUBBLEGUM
- Product NDC
- 62007-104
- 11-digit product format
- 620070104
- Labeler code
- 62007
- Product ID
- 62007-104_4a4eba66-89c2-4e49-86a2-cfb90be342bd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FLUORIDE TREATMENT
- Dosage form
- AEROSOL, FOAM
- 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 |
|---|
| 62007-104-07 | PCXX NEUTRAL FOAM BAZOOKA BUBBLEGUM | 1 mg in 1 CAN | AEROSOL, FOAM | 1 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 62007-104 | PCXX NEUTRAL FOAM BAZOOKA BUBBLEGUM (FLUORIDE TREATMENT) AEROSOL, FOAM [ROSS HEALTHCARE INC.] | 1 | Legacy NDC, 1 package rows | 20140606_7148b3ba-9626-4b0b-b6b3-000174b653d2.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 62007-104-07 | 62007010407 | 1 mg in 1 CAN | 1 mg | Historical |