Product NDC: | 54473-205 |
Proprietary Name: | Sensitive |
Non Proprietary Name: | Potassium Nitrate and Sodium Fluoride |
Active Ingredient(s): | 5.4; .26244 g/108g; g/108g & nbsp; Potassium Nitrate and Sodium Fluoride |
Administration Route(s): | TOPICAL |
Dosage Form(s): | PASTE, DENTIFRICE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54473-205 |
Labeler Name: | Melaleuca, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part356 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20120103 |
Package NDC: | 54473-205-04 |
Package Description: | 108 g in 1 TUBE (54473-205-04) |
NDC Code | 54473-205-04 |
Proprietary Name | Sensitive |
Package Description | 108 g in 1 TUBE (54473-205-04) |
Product NDC | 54473-205 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Potassium Nitrate and Sodium Fluoride |
Dosage Form Name | PASTE, DENTIFRICE |
Route Name | TOPICAL |
Start Marketing Date | 20120103 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Melaleuca, Inc. |
Substance Name | POTASSIUM NITRATE; SODIUM FLUORIDE |
Strength Number | 5.4; .26244 |
Strength Unit | g/108g; g/108g |
Pharmaceutical Classes |