SENSODYNE - 0135-0484-01 - (potassium nitrate and sodium fluoride)

Alphabetical Index


Drug Information of SENSODYNE

Product NDC: 0135-0484
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): ORAL
Dosage Form(s): PASTE
Coding System: National Drug Codes(NDC)

Labeler Information of SENSODYNE

Product NDC: 0135-0484
Labeler Name: GlaxoSmithKline Consumer Healthcare LP
Product Type: HUMAN OTC DRUG
FDA Application Number: part356
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20101018

Package Information of SENSODYNE

Package NDC: 0135-0484-01
Package Description: 113 g in 1 TUBE (0135-0484-01)

NDC Information of SENSODYNE

NDC Code 0135-0484-01
Proprietary Name SENSODYNE
Package Description 113 g in 1 TUBE (0135-0484-01)
Product NDC 0135-0484
Product Type Name HUMAN OTC DRUG
Non Proprietary Name potassium nitrate and sodium fluoride
Dosage Form Name PASTE
Route Name ORAL
Start Marketing Date 20101018
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