Denti-Care Denti-Pro

Product NDC
64778-0214
11-digit product format
647780214
Labeler code
64778
Product ID
64778-0214_7e40fae9-b3eb-49c9-e053-2991aa0a21b3
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
2020-12-31
Substance
SODIUM FLUORIDE
Active strength
0 g/mL
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record