Anticavity - 53942-163-86 - (SODIUM FLUORIDE)

Alphabetical Index


Drug Information of Anticavity

Product NDC: 53942-163
Proprietary Name: Anticavity
Non Proprietary Name: SODIUM FLUORIDE
Active Ingredient(s): 999.5    mL/100L & nbsp;   SODIUM FLUORIDE
Administration Route(s): ORAL
Dosage Form(s): MOUTHWASH
Coding System: National Drug Codes(NDC)

Labeler Information of Anticavity

Product NDC: 53942-163
Labeler Name: Demoulas Super Markets, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part355
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20060513

Package Information of Anticavity

Package NDC: 53942-163-86
Package Description: 1 L in 1 BOTTLE, PLASTIC (53942-163-86)

NDC Information of Anticavity

NDC Code 53942-163-86
Proprietary Name Anticavity
Package Description 1 L in 1 BOTTLE, PLASTIC (53942-163-86)
Product NDC 53942-163
Product Type Name HUMAN OTC DRUG
Non Proprietary Name SODIUM FLUORIDE
Dosage Form Name MOUTHWASH
Route Name ORAL
Start Marketing Date 20060513
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Demoulas Super Markets, Inc.
Substance Name SODIUM FLUORIDE
Strength Number 999.5
Strength Unit mL/100L
Pharmaceutical Classes

Complete Information of Anticavity


General Information