Denti-Care Denti-Pro
- Product NDC
- 64778-0215
- 11-digit product format
- 647780215
- Labeler code
- 64778
- Product ID
- 64778-0215_7e1fd16b-5ccf-7922-e053-2991aa0a5133
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium Fluoride
- Dosage form
- GEL
- Route
- DENTAL
- Labeler
- AMD Medicom Inc.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 1999-10-01
- Marketing end
- 0000-00-00
- Substance
- SODIUM FLUORIDE
- Active strength
- 0 g/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record