Product NDC: | 60258-150 |
Proprietary Name: | SF 5000 Plus |
Non Proprietary Name: | 1.1% Sodium Fluoride Prescription Dental Cream |
Active Ingredient(s): | 11 mg/g & nbsp; 1.1% Sodium Fluoride Prescription Dental Cream |
Administration Route(s): | DENTAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 60258-150 |
Labeler Name: | Cypress Pharmaceutical, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 19991112 |
Package NDC: | 60258-150-01 |
Package Description: | 1 TUBE in 1 CARTON (60258-150-01) > 51 g in 1 TUBE |
NDC Code | 60258-150-01 |
Proprietary Name | SF 5000 Plus |
Package Description | 1 TUBE in 1 CARTON (60258-150-01) > 51 g in 1 TUBE |
Product NDC | 60258-150 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | 1.1% Sodium Fluoride Prescription Dental Cream |
Dosage Form Name | CREAM |
Route Name | DENTAL |
Start Marketing Date | 19991112 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Cypress Pharmaceutical, Inc. |
Substance Name | SODIUM FLUORIDE |
Strength Number | 11 |
Strength Unit | mg/g |
Pharmaceutical Classes |