Pro-Den Rx

Product NDC
59883-820
11-digit product format
598830820
Labeler code
59883
Product ID
59883-820_82f9290a-dfa2-1ba2-e053-2991aa0a41f4
Type
HUMAN OTC DRUG
Nonproprietary name
Sodium Fluoride
Dosage form
GEL
Route
ORAL
Labeler
DEN-MAT HOLDINGS, LLC
Application
part355
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2008-10-31
Marketing end
0000-00-00
Substance
SODIUM FLUORIDE
Active strength
4 g/g
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59883-820PRO-DEN RX (SODIUM FLUORIDE) GEL [DEN-MAT HOLDINGS, LLC]2Legacy NDC20190301_57080023-c62b-4bbe-a76c-ed7ae576640f.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
59883-820-02598830820021 TUBE in 1 CARTON (59883-820-02) > 56 g in 1 TUBE1 tube2008-10-310000-00-00NoNoCurrent