Denti-Care Denti-Foam

Product NDC
64778-0375
11-digit product format
647780375
Labeler code
64778
Product ID
64778-0375_b60e3e37-96c8-9dac-e053-2a95a90a2d01
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
2003-04-01
Marketing end
2021-12-31
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

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
64778-0375-36477803750312 BOTTLE, SPRAY in 1 CASE (64778-0375-3) > 125 g in 1 BOTTLE, SPRAY (64778-0375-1) 2017-12-012021-12-31NoNoCurrent