Product NDC: | 60258-158 |
Proprietary Name: | Neutral Sodium Fluoride 0.2% |
Non Proprietary Name: | sodium fluoride |
Active Ingredient(s): | 9 mg/10mL & nbsp; sodium fluoride |
Administration Route(s): | ORAL |
Dosage Form(s): | RINSE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 60258-158 |
Labeler Name: | Cypress Pharmaceutical, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED OTHER |
Start Marketing Date: | 20060801 |
Package NDC: | 60258-158-16 |
Package Description: | 473 mL in 1 BOTTLE, PLASTIC (60258-158-16) |
NDC Code | 60258-158-16 |
Proprietary Name | Neutral Sodium Fluoride 0.2% |
Package Description | 473 mL in 1 BOTTLE, PLASTIC (60258-158-16) |
Product NDC | 60258-158 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | sodium fluoride |
Dosage Form Name | RINSE |
Route Name | ORAL |
Start Marketing Date | 20060801 |
Marketing Category Name | UNAPPROVED OTHER |
Labeler Name | Cypress Pharmaceutical, Inc. |
Substance Name | SODIUM FLUORIDE |
Strength Number | 9 |
Strength Unit | mg/10mL |
Pharmaceutical Classes |