NDC 0135-0460
SENSODYNE PRONAMEL Daily Protection
Potassium Nitrate And Sodium Fluoride
SENSODYNE PRONAMEL Daily Protection 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 | 0135-0460_18c10f35-44a1-4a2b-a1ad-56a7e7674767 |
| NDC | 0135-0460 |
| Product Type | Human Otc Drug |
| Proprietary Name | SENSODYNE PRONAMEL Daily Protection |
| Generic Name | Potassium Nitrate And Sodium Fluoride |
| Dosage Form | Paste |
| Route of Administration | ORAL |
| Marketing Start Date | 2010-10-18 |
| 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 |
Packaging
NDC 0135-0460-01
1 TUBE in 1 CARTON (0135-0460-01) > 113 g in 1 TUBE
| Marketing Start Date | 2010-10-18 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 0135-0460-03 [00135046003]
SENSODYNE PRONAMEL Daily Protection PASTE
| Marketing Category | OTC monograph not final |
| Application Number | part356 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2010-10-18 |
NDC 0135-0460-06 [00135046006]
SENSODYNE PRONAMEL Daily Protection PASTE
| Marketing Category | OTC monograph not final |
| Application Number | part356 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2017-11-29 |
NDC 0135-0460-02 [00135046002]
SENSODYNE PRONAMEL Daily Protection PASTE
| Marketing Category | OTC monograph not final |
| Application Number | part356 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2010-10-18 |
| Marketing End Date | 2017-12-21 |
NDC 0135-0460-01 [00135046001]
SENSODYNE PRONAMEL Daily Protection PASTE
| Marketing Category | OTC monograph not final |
| Application Number | part356 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2010-10-18 |
Drug Details
Active Ingredients
| Ingredient | Strength |
|---|---|
| POTASSIUM NITRATE | 50 mg/g |
NDC Crossover Matching brand name "SENSODYNE PRONAMEL Daily Protection" or generic name "Potassium Nitrate And Sodium Fluoride"
| NDC | Brand Name | Generic Name |
|---|---|---|
| 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 |
Trademark Results [SENSODYNE PRONAMEL]
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 |
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