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 |