Product NDC: | 48878-3315 |
Proprietary Name: | PerioMed |
Non Proprietary Name: | stannous fluoride |
Active Ingredient(s): | 6.3 mg/g & nbsp; stannous fluoride |
Administration Route(s): | ORAL |
Dosage Form(s): | RINSE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 48878-3315 |
Labeler Name: | 3M ESPE Dental Products |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part355 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 19670701 |
Package NDC: | 48878-3315-0 |
Package Description: | 1 BOTTLE, PLASTIC in 1 BOX (48878-3315-0) > 283.5 g in 1 BOTTLE, PLASTIC |
NDC Code | 48878-3315-0 |
Proprietary Name | PerioMed |
Package Description | 1 BOTTLE, PLASTIC in 1 BOX (48878-3315-0) > 283.5 g in 1 BOTTLE, PLASTIC |
Product NDC | 48878-3315 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | stannous fluoride |
Dosage Form Name | RINSE |
Route Name | ORAL |
Start Marketing Date | 19670701 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | 3M ESPE Dental Products |
Substance Name | STANNOUS FLUORIDE |
Strength Number | 6.3 |
Strength Unit | mg/g |
Pharmaceutical Classes |