Product NDC: | 41520-878 |
Proprietary Name: | PEANUTS ANTI-CAVITY FLUORIDE TOOTHPASTE |
Non Proprietary Name: | SODIUM FLUORIDE |
Active Ingredient(s): | .24 g/100g & nbsp; SODIUM FLUORIDE |
Administration Route(s): | DENTAL |
Dosage Form(s): | PASTE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 41520-878 |
Labeler Name: | American Sales Company |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part355 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100913 |
Package NDC: | 41520-878-14 |
Package Description: | 119 g in 1 TUBE (41520-878-14) |
NDC Code | 41520-878-14 |
Proprietary Name | PEANUTS ANTI-CAVITY FLUORIDE TOOTHPASTE |
Package Description | 119 g in 1 TUBE (41520-878-14) |
Product NDC | 41520-878 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | SODIUM FLUORIDE |
Dosage Form Name | PASTE |
Route Name | DENTAL |
Start Marketing Date | 20100913 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | American Sales Company |
Substance Name | SODIUM FLUORIDE |
Strength Number | .24 |
Strength Unit | g/100g |
Pharmaceutical Classes |