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Opalescence PF - 51206-303-07 - (Sodium Fluoride and Potassium Nitrate)

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Drug Information of Opalescence PF

Product NDC: 51206-303
Proprietary Name: Opalescence PF
Non Proprietary Name: Sodium Fluoride and Potassium Nitrate
Active Ingredient(s): 1.4175; .070875    g/28.35g; g/28.35g & nbsp;   Sodium Fluoride and Potassium Nitrate
Administration Route(s): DENTAL
Dosage Form(s): PASTE, DENTIFRICE
Coding System: National Drug Codes(NDC)

Labeler Information of Opalescence PF

Product NDC: 51206-303
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 PF

Package NDC: 51206-303-07
Package Description: 1 TUBE in 1 BOX (51206-303-07) > 28.35 g in 1 TUBE

NDC Information of Opalescence PF

NDC Code 51206-303-07
Proprietary Name Opalescence PF
Package Description 1 TUBE in 1 BOX (51206-303-07) > 28.35 g in 1 TUBE
Product NDC 51206-303
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Sodium Fluoride and Potassium Nitrate
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 POTASSIUM NITRATE; SODIUM FLUORIDE
Strength Number 1.4175; .070875
Strength Unit g/28.35g; g/28.35g
Pharmaceutical Classes

Complete Information of Opalescence PF


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