Product NDC: | 46437-001 |
Proprietary Name: | Tanda pearl professional whitening |
Non Proprietary Name: | Sodium Fluoride |
Active Ingredient(s): | .33 g/133g & nbsp; Sodium Fluoride |
Administration Route(s): | DENTAL |
Dosage Form(s): | PASTE, DENTIFRICE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 46437-001 |
Labeler Name: | Syneron Beauty Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part355 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120803 |
Package NDC: | 46437-001-01 |
Package Description: | 1 TUBE in 1 BOX (46437-001-01) > 133 g in 1 TUBE |
NDC Code | 46437-001-01 |
Proprietary Name | Tanda pearl professional whitening |
Package Description | 1 TUBE in 1 BOX (46437-001-01) > 133 g in 1 TUBE |
Product NDC | 46437-001 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Sodium Fluoride |
Dosage Form Name | PASTE, DENTIFRICE |
Route Name | DENTAL |
Start Marketing Date | 20120803 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Syneron Beauty Inc. |
Substance Name | SODIUM FLUORIDE |
Strength Number | .33 |
Strength Unit | g/133g |
Pharmaceutical Classes |