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Anticavity Fluoride - 59779-213-44 - (Sodium Fluoride)

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Drug Information of Anticavity Fluoride

Product NDC: 59779-213
Proprietary Name: Anticavity Fluoride
Non Proprietary Name: Sodium Fluoride
Active Ingredient(s): .05    kg/100L & nbsp;   Sodium Fluoride
Administration Route(s): ORAL
Dosage Form(s): RINSE
Coding System: National Drug Codes(NDC)

Labeler Information of Anticavity Fluoride

Product NDC: 59779-213
Labeler Name: CVS Pharmacy, Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part355
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20010619

Package Information of Anticavity Fluoride

Package NDC: 59779-213-44
Package Description: .5 L in 1 BOTTLE, PLASTIC (59779-213-44)

NDC Information of Anticavity Fluoride

NDC Code 59779-213-44
Proprietary Name Anticavity Fluoride
Package Description .5 L in 1 BOTTLE, PLASTIC (59779-213-44)
Product NDC 59779-213
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Sodium Fluoride
Dosage Form Name RINSE
Route Name ORAL
Start Marketing Date 20010619
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name CVS Pharmacy, Inc
Substance Name SODIUM FLUORIDE
Strength Number .05
Strength Unit kg/100L
Pharmaceutical Classes

Complete Information of Anticavity Fluoride


General Information