SENSODYNE - 0135-0548-02 - (stannous fluoride)

Alphabetical Index


Drug Information of SENSODYNE

Product NDC: 0135-0548
Proprietary Name: SENSODYNE
Non Proprietary Name: stannous fluoride
Active Ingredient(s): 1.5    mg/g & nbsp;   stannous fluoride
Administration Route(s): ORAL
Dosage Form(s): PASTE
Coding System: National Drug Codes(NDC)

Labeler Information of SENSODYNE

Product NDC: 0135-0548
Labeler Name: GlaxoSmithKline Consumer Healthcare LP
Product Type: HUMAN OTC DRUG
FDA Application Number: part356
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20130204

Package Information of SENSODYNE

Package NDC: 0135-0548-02
Package Description: 1 TUBE in 1 CARTON (0135-0548-02) > 96.4 g in 1 TUBE

NDC Information of SENSODYNE

NDC Code 0135-0548-02
Proprietary Name SENSODYNE
Package Description 1 TUBE in 1 CARTON (0135-0548-02) > 96.4 g in 1 TUBE
Product NDC 0135-0548
Product Type Name HUMAN OTC DRUG
Non Proprietary Name stannous fluoride
Dosage Form Name PASTE
Route Name ORAL
Start Marketing Date 20130204
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name GlaxoSmithKline Consumer Healthcare LP
Substance Name STANNOUS FLUORIDE
Strength Number 1.5
Strength Unit mg/g
Pharmaceutical Classes

Complete Information of SENSODYNE


General Information