Supersmile - 53567-0717-5 - (Sodium Monofluorophosphate)

Alphabetical Index


Drug Information of Supersmile

Product NDC: 53567-0717
Proprietary Name: Supersmile
Non Proprietary Name: Sodium Monofluorophosphate
Active Ingredient(s): 1.4    mg/g & nbsp;   Sodium Monofluorophosphate
Administration Route(s): DENTAL; ORAL
Dosage Form(s): PASTE, DENTIFRICE
Coding System: National Drug Codes(NDC)

Labeler Information of Supersmile

Product NDC: 53567-0717
Labeler Name: Robell Research, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part355
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20060101

Package Information of Supersmile

Package NDC: 53567-0717-5
Package Description: 14.2 g in 1 TUBE (53567-0717-5)

NDC Information of Supersmile

NDC Code 53567-0717-5
Proprietary Name Supersmile
Package Description 14.2 g in 1 TUBE (53567-0717-5)
Product NDC 53567-0717
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Sodium Monofluorophosphate
Dosage Form Name PASTE, DENTIFRICE
Route Name DENTAL; ORAL
Start Marketing Date 20060101
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Robell Research, Inc.
Substance Name SODIUM MONOFLUOROPHOSPHATE
Strength Number 1.4
Strength Unit mg/g
Pharmaceutical Classes

Complete Information of Supersmile


General Information