Denti-Care Denti-Foam

Product NDC
64778-0378
11-digit product format
647780378
Labeler code
64778
Product ID
64778-0378_7e9203d2-c833-76f0-e053-2a91aa0a305a
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Sodium Fluoride
Dosage form
AEROSOL, FOAM
Route
DENTAL
Labeler
AMD Medicom Inc
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2005-05-01
Marketing end
2020-12-31
Substance
SODIUM FLUORIDE
Active strength
0 g/g
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record