Sensodyne Pronamel Strong and Bright Enamel Mint is a Oral Paste in the Human Otc Drug category. It is labeled and distributed by Glaxosmithkline Consumer Healthcare Holdings (us) Llc. The primary component is Potassium Nitrate; Sodium Fluoride.
| Product ID | 0135-0602_12961035-ae7c-47f0-9190-46a212718152 | 
| NDC | 0135-0602 | 
| Product Type | Human Otc Drug | 
| Proprietary Name | Sensodyne Pronamel Strong and Bright Enamel Mint | 
| Generic Name | Potassium Nitrate And Sodium Fluoride | 
| Dosage Form | Paste | 
| Route of Administration | ORAL | 
| Marketing Start Date | 2016-12-19 | 
| Marketing Category | OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL | 
| Application Number | part356 | 
| Labeler Name | GlaxoSmithKline Consumer Healthcare Holdings (US) LLC | 
| Substance Name | POTASSIUM NITRATE; SODIUM FLUORIDE | 
| Active Ingredient Strength | 50 mg/g; mg/g | 
| NDC Exclude Flag | N | 
| Listing Certified Through | 2020-12-31 | 
| Marketing Start Date | 2016-12-19 | 
| NDC Exclude Flag | N | 
| Sample Package? | N | 
| Marketing Category | OTC monograph not final | 
| Application Number | part356 | 
| Product Type | HUMAN OTC DRUG | 
| Billing Unit | GM | 
| Marketing Start Date | 2016-12-19 | 
| Marketing Category | OTC monograph not final | 
| Application Number | part356 | 
| Product Type | HUMAN OTC DRUG | 
| Marketing Start Date | 2016-12-19 | 
| Ingredient | Strength | 
|---|---|
| POTASSIUM NITRATE | 50 mg/g | 
| SPL SET ID: | be1ae382-0e01-4db8-90d7-fdadec2ff861 | 
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | 
| NDC | Brand Name | Generic Name | 
|---|---|---|
| 0135-0602 | Sensodyne Pronamel Strong and Bright Enamel Mint | Sensodyne Pronamel Strong and Bright Enamel Mint | 
| 0135-0525 | Sensodyne | potassium nitrate and sodium fluoride | 
| 0135-0526 | Sensodyne | potassium nitrate and sodium fluoride | 
| 0135-0527 | Sensodyne | potassium nitrate and sodium fluoride | 
| 0135-0528 | Sensodyne | potassium nitrate and sodium fluoride | 
| 0135-0450 | SENSODYNE PRONAMEL | potassium nitrate and sodium fluoride | 
| 0135-0460 | SENSODYNE PRONAMEL | potassium nitrate and sodium fluoride | 
| 0135-0480 | SENSODYNE PRONAMEL | potassium nitrate and sodium fluoride | 
| 0135-0481 | SENSODYNE PRONAMEL | potassium nitrate and sodium fluoride | 
| 0135-0484 | SENSODYNE PRONAMEL | potassium nitrate and sodium fluoride | 
| 0135-0486 | SENSODYNE PRONAMEL | potassium nitrate and sodium fluoride | 
| 0135-0492 | SENSODYNE PRONAMEL | potassium nitrate and sodium fluoride | 
| 0135-0520 | SENSODYNE PRONAMEL | potassium nitrate and sodium fluoride | 
| Mark Image Registration | Serial | Company Trademark Application Date | 
|---|---|
|  SENSODYNE PRONAMEL  78979618  3393575 Live/Registered | BLOCK DRUG COMPANY, INC. 2005-10-21 | 
|  SENSODYNE PRONAMEL  78738283  not registered Dead/Abandoned | SMITHKLINE BEECHAM CORPORATION 2005-10-21 |