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