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Sensodyne Pronamel
Sensodyne Pronamel - 0135-0549-01 - (sodium fluoride)
Drug Information of Sensodyne Pronamel
| Product NDC: | 0135-0549 |
| Proprietary Name: | Sensodyne Pronamel |
| Non Proprietary Name: | sodium fluoride |
| Active Ingredient(s): | .2 mg/L & nbsp; sodium fluoride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | MOUTHWASH |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sensodyne Pronamel
| Product NDC: | 0135-0549 |
| Labeler Name: | GlaxoSmithKline Consumer Healthcare LP |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part355 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130204 |
Package Information of Sensodyne Pronamel
| Package NDC: | 0135-0549-01 |
| Package Description: | .25 L in 1 BOTTLE (0135-0549-01) |
NDC Information of Sensodyne Pronamel
| NDC Code | 0135-0549-01 |
| Proprietary Name | Sensodyne Pronamel |
| Package Description | .25 L in 1 BOTTLE (0135-0549-01) |
| Product NDC | 0135-0549 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | sodium fluoride |
| Dosage Form Name | MOUTHWASH |
| Route Name | ORAL |
| Start Marketing Date | 20130204 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | GlaxoSmithKline Consumer Healthcare LP |
| Substance Name | SODIUM FLUORIDE |
| Strength Number | .2 |
| Strength Unit | mg/L |
| Pharmaceutical Classes |
