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Dawnmist Fluoride - 65517-1000-2 - (SODIUM MONOFLUOROPHOSPHATE)

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Drug Information of Dawnmist Fluoride

Product NDC: 65517-1000
Proprietary Name: Dawnmist Fluoride
Non Proprietary Name: SODIUM MONOFLUOROPHOSPHATE
Active Ingredient(s): .76    g/100g & nbsp;   SODIUM MONOFLUOROPHOSPHATE
Administration Route(s): DENTAL
Dosage Form(s): PASTE
Coding System: National Drug Codes(NDC)

Labeler Information of Dawnmist Fluoride

Product NDC: 65517-1000
Labeler Name: Dukal Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: part355
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20120924

Package Information of Dawnmist Fluoride

Package NDC: 65517-1000-2
Package Description: 42 g in 1 TUBE (65517-1000-2)

NDC Information of Dawnmist Fluoride

NDC Code 65517-1000-2
Proprietary Name Dawnmist Fluoride
Package Description 42 g in 1 TUBE (65517-1000-2)
Product NDC 65517-1000
Product Type Name HUMAN OTC DRUG
Non Proprietary Name SODIUM MONOFLUOROPHOSPHATE
Dosage Form Name PASTE
Route Name DENTAL
Start Marketing Date 20120924
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Dukal Corporation
Substance Name SODIUM MONOFLUOROPHOSPHATE
Strength Number .76
Strength Unit g/100g
Pharmaceutical Classes

Complete Information of Dawnmist Fluoride


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