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Opalescence Plus - 51206-304-06 - (Sodium Fluoride)

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Drug Information of Opalescence Plus

Product NDC: 51206-304
Proprietary Name: Opalescence Plus
Non Proprietary Name: Sodium Fluoride
Active Ingredient(s): .070875    g/28.35g & nbsp;   Sodium Fluoride
Administration Route(s): DENTAL
Dosage Form(s): PASTE, DENTIFRICE
Coding System: National Drug Codes(NDC)

Labeler Information of Opalescence Plus

Product NDC: 51206-304
Labeler Name: Ultradent Products, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part355
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20101115

Package Information of Opalescence Plus

Package NDC: 51206-304-06
Package Description: 1 TUBE in 1 BOX (51206-304-06) > 133 g in 1 TUBE

NDC Information of Opalescence Plus

NDC Code 51206-304-06
Proprietary Name Opalescence Plus
Package Description 1 TUBE in 1 BOX (51206-304-06) > 133 g in 1 TUBE
Product NDC 51206-304
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Sodium Fluoride
Dosage Form Name PASTE, DENTIFRICE
Route Name DENTAL
Start Marketing Date 20101115
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Ultradent Products, Inc.
Substance Name SODIUM FLUORIDE
Strength Number .070875
Strength Unit g/28.35g
Pharmaceutical Classes

Complete Information of Opalescence Plus


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