Sensodyne - 10158-985-50 - (potassium nitrate and sodium fluoride)

Alphabetical Index


Drug Information of Sensodyne

Product NDC: 10158-985
Proprietary Name: Sensodyne
Non Proprietary Name: potassium nitrate and sodium fluoride
Active Ingredient(s): 50; 1.5    mg/g; mg/g & nbsp;   potassium nitrate and sodium fluoride
Administration Route(s): DENTAL
Dosage Form(s): PASTE
Coding System: National Drug Codes(NDC)

Labeler Information of Sensodyne

Product NDC: 10158-985
Labeler Name: GlaxoSmithKline Consumer Healthcare LP
Product Type: HUMAN OTC DRUG
FDA Application Number: part356
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20110608

Package Information of Sensodyne

Package NDC: 10158-985-50
Package Description: 1 TUBE in 1 CARTON (10158-985-50) > 113 g in 1 TUBE

NDC Information of Sensodyne

NDC Code 10158-985-50
Proprietary Name Sensodyne
Package Description 1 TUBE in 1 CARTON (10158-985-50) > 113 g in 1 TUBE
Product NDC 10158-985
Product Type Name HUMAN OTC DRUG
Non Proprietary Name potassium nitrate and sodium fluoride
Dosage Form Name PASTE
Route Name DENTAL
Start Marketing Date 20110608
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name GlaxoSmithKline Consumer Healthcare LP
Substance Name POTASSIUM NITRATE; SODIUM FLUORIDE
Strength Number 50; 1.5
Strength Unit mg/g; mg/g
Pharmaceutical Classes

Complete Information of Sensodyne


General Information