Product NDC: | 51009-166 |
Proprietary Name: | Maximum Strength Sensitive |
Non Proprietary Name: | Sodium Fluoride and Potassium Nitrate |
Active Ingredient(s): | .05; .00243 g/g; g/g & nbsp; Sodium Fluoride and Potassium Nitrate |
Administration Route(s): | DENTAL |
Dosage Form(s): | PASTE, DENTIFRICE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51009-166 |
Labeler Name: | Tom's of Maine, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part355 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20090901 |
Package NDC: | 51009-166-04 |
Package Description: | 1 TUBE in 1 BOX (51009-166-04) > 113 g in 1 TUBE |
NDC Code | 51009-166-04 |
Proprietary Name | Maximum Strength Sensitive |
Package Description | 1 TUBE in 1 BOX (51009-166-04) > 113 g in 1 TUBE |
Product NDC | 51009-166 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Sodium Fluoride and Potassium Nitrate |
Dosage Form Name | PASTE, DENTIFRICE |
Route Name | DENTAL |
Start Marketing Date | 20090901 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Tom's of Maine, Inc. |
Substance Name | POTASSIUM NITRATE; SODIUM FLUORIDE |
Strength Number | .05; .00243 |
Strength Unit | g/g; g/g |
Pharmaceutical Classes |