Aquafresh - 0135-0219-08 - (sodium monofluorophosphate)

Alphabetical Index


Drug Information of Aquafresh

Product NDC: 0135-0219
Proprietary Name: Aquafresh
Non Proprietary Name: sodium monofluorophosphate
Active Ingredient(s): 1.5    mg/g & nbsp;   sodium monofluorophosphate
Administration Route(s): DENTAL
Dosage Form(s): PASTE
Coding System: National Drug Codes(NDC)

Labeler Information of Aquafresh

Product NDC: 0135-0219
Labeler Name: GlaxoSmithKline Consumer Healthcare LP
Product Type: HUMAN OTC DRUG
FDA Application Number: part355
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20110128

Package Information of Aquafresh

Package NDC: 0135-0219-08
Package Description: 1 TUBE in 1 CARTON (0135-0219-08) > 99.2 g in 1 TUBE

NDC Information of Aquafresh

NDC Code 0135-0219-08
Proprietary Name Aquafresh
Package Description 1 TUBE in 1 CARTON (0135-0219-08) > 99.2 g in 1 TUBE
Product NDC 0135-0219
Product Type Name HUMAN OTC DRUG
Non Proprietary Name sodium monofluorophosphate
Dosage Form Name PASTE
Route Name DENTAL
Start Marketing Date 20110128
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name GlaxoSmithKline Consumer Healthcare LP
Substance Name SODIUM MONOFLUOROPHOSPHATE
Strength Number 1.5
Strength Unit mg/g
Pharmaceutical Classes

Complete Information of Aquafresh


General Information