PCXX Home Treatment 1.1
- Product NDC
- 62007-035
- 11-digit product format
- 620070035
- Labeler code
- 62007
- Product ID
- 62007-035_83d5b9dd-43ae-685e-e053-2a91aa0a1dbc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- SODIUM FLUORIDE
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Ross Healthcare Inc.
- Marketing category
- UNAPPROVED DRUG
- Marketing start
- 2015-02-16
- Marketing end
- 0000-00-00
- Substance
- SODIUM FLUORIDE
- Active strength
- 11 mg/mg
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record