Product NDC: | 63783-210 |
Proprietary Name: | GINGIMED |
Non Proprietary Name: | STANNOUS FLUORIDE |
Active Ingredient(s): | .71034 g/120g & nbsp; STANNOUS FLUORIDE |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63783-210 |
Labeler Name: | Massco Dental A Division of Dunagin Pharmaceuticals |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | part355 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 19890101 |
Package NDC: | 63783-210-06 |
Package Description: | 120 g in 1 BOTTLE, WITH APPLICATOR (63783-210-06) |
NDC Code | 63783-210-06 |
Proprietary Name | GINGIMED |
Package Description | 120 g in 1 BOTTLE, WITH APPLICATOR (63783-210-06) |
Product NDC | 63783-210 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | STANNOUS FLUORIDE |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 19890101 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Massco Dental A Division of Dunagin Pharmaceuticals |
Substance Name | STANNOUS FLUORIDE |
Strength Number | .71034 |
Strength Unit | g/120g |
Pharmaceutical Classes |