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SENSODYNE
SENSODYNE - 0135-0519-01 - (potassium nitrate and sodium fluoride)
Drug Information of SENSODYNE
| Product NDC: | 0135-0519 |
| 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): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SENSODYNE
| Product NDC: | 0135-0519 |
| Labeler Name: | GlaxoSmithKline Consumer Healthcare LP |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part356 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110614 |
Package Information of SENSODYNE
| Package NDC: | 0135-0519-01 |
| Package Description: | 121.6 g in 1 CAN (0135-0519-01) |
NDC Information of SENSODYNE
| NDC Code | 0135-0519-01 |
| Proprietary Name | SENSODYNE |
| Package Description | 121.6 g in 1 CAN (0135-0519-01) |
| Product NDC | 0135-0519 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | potassium nitrate and sodium fluoride |
| Dosage Form Name | GEL |
| Route Name | DENTAL |
| Start Marketing Date | 20110614 |
| 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 |
