PROPOLIS - 52257-1209-1 - (SODIUM MONOFLUOROPHOSPHATE, SODIUM FLUORIDE)

Alphabetical Index


Drug Information of PROPOLIS

Product NDC: 52257-1209
Proprietary Name: PROPOLIS
Non Proprietary Name: SODIUM MONOFLUOROPHOSPHATE, SODIUM FLUORIDE
Active Ingredient(s): .2; .32    g/200g; g/200g & nbsp;   SODIUM MONOFLUOROPHOSPHATE, SODIUM FLUORIDE
Administration Route(s): DENTAL
Dosage Form(s): PASTE, DENTIFRICE
Coding System: National Drug Codes(NDC)

Labeler Information of PROPOLIS

Product NDC: 52257-1209
Labeler Name: ATOMY CO., LTD.
Product Type: HUMAN OTC DRUG
FDA Application Number: part355
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100525

Package Information of PROPOLIS

Package NDC: 52257-1209-1
Package Description: 200 g in 1 CARTON (52257-1209-1)

NDC Information of PROPOLIS

NDC Code 52257-1209-1
Proprietary Name PROPOLIS
Package Description 200 g in 1 CARTON (52257-1209-1)
Product NDC 52257-1209
Product Type Name HUMAN OTC DRUG
Non Proprietary Name SODIUM MONOFLUOROPHOSPHATE, SODIUM FLUORIDE
Dosage Form Name PASTE, DENTIFRICE
Route Name DENTAL
Start Marketing Date 20100525
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name ATOMY CO., LTD.
Substance Name SODIUM FLUORIDE; SODIUM MONOFLUOROPHOSPHATE
Strength Number .2; .32
Strength Unit g/200g; g/200g
Pharmaceutical Classes

Complete Information of PROPOLIS


General Information