| Product NDC: | 11822-0001 |
| Proprietary Name: | Rite Aid Anti-Cavity, Anti-Gingivitis |
| Non Proprietary Name: | Stannous Fluoride |
| Active Ingredient(s): | 4.54 mg/g & nbsp; Stannous Fluoride |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | PASTE |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 11822-0001 |
| Labeler Name: | Rite Aid |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part355 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20101208 |
| Package NDC: | 11822-0001-1 |
| Package Description: | 170 g in 1 TUBE (11822-0001-1) |
| NDC Code | 11822-0001-1 |
| Proprietary Name | Rite Aid Anti-Cavity, Anti-Gingivitis |
| Package Description | 170 g in 1 TUBE (11822-0001-1) |
| Product NDC | 11822-0001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Stannous Fluoride |
| Dosage Form Name | PASTE |
| Route Name | DENTAL |
| Start Marketing Date | 20101208 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Rite Aid |
| Substance Name | STANNOUS FLUORIDE |
| Strength Number | 4.54 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |