| Product NDC: | 55346-0402 |
| Proprietary Name: | Alpha-dent |
| 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: | 55346-0402 |
| 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: | 55346-0402-1 |
| Package Description: | 121.9 g in 1 TUBE (55346-0402-1) |
| NDC Code | 55346-0402-1 |
| Proprietary Name | Alpha-dent |
| Package Description | 121.9 g in 1 TUBE (55346-0402-1) |
| Product NDC | 55346-0402 |
| 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 |