Neutral Topical

Product NDC
64778-0388
11-digit product format
647780388
Labeler code
64778
Product ID
64778-0388_b60e23f9-0639-3796-e053-2a95a90a19f5
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
2004-12-01
Marketing end
2021-09-30
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
64778-0388-36477803880312 BOTTLE, SPRAY in 1 CASE (64778-0388-3) > 125 g in 1 BOTTLE, SPRAY (64778-0388-1) 2017-12-012021-09-30NoNoCurrent