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ADVANCED FLUORIDE ANTICAVITY - 29500-0819-6 - (SODIUM MONOFLUOROPHOSPHATE)

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Drug Information of ADVANCED FLUORIDE ANTICAVITY

Product NDC: 29500-0819
Proprietary Name: ADVANCED FLUORIDE ANTICAVITY
Non Proprietary Name: SODIUM MONOFLUOROPHOSPHATE
Active Ingredient(s): .76    g/100g & nbsp;   SODIUM MONOFLUOROPHOSPHATE
Administration Route(s): DENTAL
Dosage Form(s): PASTE, DENTIFRICE
Coding System: National Drug Codes(NDC)

Labeler Information of ADVANCED FLUORIDE ANTICAVITY

Product NDC: 29500-0819
Labeler Name: Personal Care Products, LLC
Product Type: HUMAN OTC DRUG
FDA Application Number: part355
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20110124

Package Information of ADVANCED FLUORIDE ANTICAVITY

Package NDC: 29500-0819-6
Package Description: 1 TUBE in 1 BOX (29500-0819-6) > 181 g in 1 TUBE

NDC Information of ADVANCED FLUORIDE ANTICAVITY

NDC Code 29500-0819-6
Proprietary Name ADVANCED FLUORIDE ANTICAVITY
Package Description 1 TUBE in 1 BOX (29500-0819-6) > 181 g in 1 TUBE
Product NDC 29500-0819
Product Type Name HUMAN OTC DRUG
Non Proprietary Name SODIUM MONOFLUOROPHOSPHATE
Dosage Form Name PASTE, DENTIFRICE
Route Name DENTAL
Start Marketing Date 20110124
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Personal Care Products, LLC
Substance Name SODIUM MONOFLUOROPHOSPHATE
Strength Number .76
Strength Unit g/100g
Pharmaceutical Classes

Complete Information of ADVANCED FLUORIDE ANTICAVITY


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