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Phos-Flur Ortho Defense - 0126-0139-16 - (SODIUM FLUORIDE)

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Drug Information of Phos-Flur Ortho Defense

Product NDC: 0126-0139
Proprietary Name: Phos-Flur Ortho Defense
Non Proprietary Name: SODIUM FLUORIDE
Active Ingredient(s): 4.42    mg/10mL & nbsp;   SODIUM FLUORIDE
Administration Route(s): DENTAL
Dosage Form(s): RINSE
Coding System: National Drug Codes(NDC)

Labeler Information of Phos-Flur Ortho Defense

Product NDC: 0126-0139
Labeler Name: Colgate Oral Pharmaceuticals, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part355
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20110211

Package Information of Phos-Flur Ortho Defense

Package NDC: 0126-0139-16
Package Description: 473 mL in 1 BOTTLE (0126-0139-16)

NDC Information of Phos-Flur Ortho Defense

NDC Code 0126-0139-16
Proprietary Name Phos-Flur Ortho Defense
Package Description 473 mL in 1 BOTTLE (0126-0139-16)
Product NDC 0126-0139
Product Type Name HUMAN OTC DRUG
Non Proprietary Name SODIUM FLUORIDE
Dosage Form Name RINSE
Route Name DENTAL
Start Marketing Date 20110211
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Colgate Oral Pharmaceuticals, Inc.
Substance Name SODIUM FLUORIDE
Strength Number 4.42
Strength Unit mg/10mL
Pharmaceutical Classes

Complete Information of Phos-Flur Ortho Defense


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