Product NDC: | 39892-0603 |
Proprietary Name: | MediChoice Premium Anticavity Fluoride |
Non Proprietary Name: | SODIUM FLUORIDE |
Active Ingredient(s): | 2.43 mg/g & nbsp; SODIUM FLUORIDE |
Administration Route(s): | DENTAL |
Dosage Form(s): | PASTE, DENTIFRICE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 39892-0603 |
Labeler Name: | Owens & Minor |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part355 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20130301 |
Package NDC: | 39892-0603-2 |
Package Description: | 24 g in 1 TUBE (39892-0603-2) |
NDC Code | 39892-0603-2 |
Proprietary Name | MediChoice Premium Anticavity Fluoride |
Package Description | 24 g in 1 TUBE (39892-0603-2) |
Product NDC | 39892-0603 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | SODIUM FLUORIDE |
Dosage Form Name | PASTE, DENTIFRICE |
Route Name | DENTAL |
Start Marketing Date | 20130301 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Owens & Minor |
Substance Name | SODIUM FLUORIDE |
Strength Number | 2.43 |
Strength Unit | mg/g |
Pharmaceutical Classes |