OraBrite - 54371-471-01 - (SODIUM FLUORIDE)

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Drug Information of OraBrite

Product NDC: 54371-471
Proprietary Name: OraBrite
Non Proprietary Name: SODIUM FLUORIDE
Active Ingredient(s): .22    g/100g & nbsp;   SODIUM FLUORIDE
Administration Route(s): DENTAL
Dosage Form(s): PASTE, DENTIFRICE
Coding System: National Drug Codes(NDC)

Labeler Information of OraBrite

Product NDC: 54371-471
Labeler Name: Oraline, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part356
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20111031

Package Information of OraBrite

Package NDC: 54371-471-01
Package Description: 24 g in 1 TUBE (54371-471-01)

NDC Information of OraBrite

NDC Code 54371-471-01
Proprietary Name OraBrite
Package Description 24 g in 1 TUBE (54371-471-01)
Product NDC 54371-471
Product Type Name HUMAN OTC DRUG
Non Proprietary Name SODIUM FLUORIDE
Dosage Form Name PASTE, DENTIFRICE
Route Name DENTAL
Start Marketing Date 20111031
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Oraline, Inc.
Substance Name SODIUM FLUORIDE
Strength Number .22
Strength Unit g/100g
Pharmaceutical Classes

Complete Information of OraBrite


General Information