Product NDC: | 55346-0404 |
Proprietary Name: | Home Care Fluoride |
Non Proprietary Name: | Stannous Fluoride |
Active Ingredient(s): | .969 mg/g & nbsp; Stannous Fluoride |
Administration Route(s): | DENTAL; ORAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55346-0404 |
Labeler Name: | Dental Technologies, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part355 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 19991231 |
Package NDC: | 55346-0404-1 |
Package Description: | 121.9 g in 1 TUBE (55346-0404-1) |
NDC Code | 55346-0404-1 |
Proprietary Name | Home Care Fluoride |
Package Description | 121.9 g in 1 TUBE (55346-0404-1) |
Product NDC | 55346-0404 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Stannous Fluoride |
Dosage Form Name | GEL |
Route Name | DENTAL; ORAL |
Start Marketing Date | 19991231 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Dental Technologies, Inc. |
Substance Name | STANNOUS FLUORIDE |
Strength Number | .969 |
Strength Unit | mg/g |
Pharmaceutical Classes |