Product NDC: | 0363-8201 |
Proprietary Name: | Walgreens |
Non Proprietary Name: | Fluoride |
Active Ingredient(s): | .76 g/100g & nbsp; Fluoride |
Administration Route(s): | DENTAL |
Dosage Form(s): | PASTE, DENTIFRICE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0363-8201 |
Labeler Name: | Walgreens |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part355 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20121001 |
Package NDC: | 0363-8201-19 |
Package Description: | 1 TUBE in 1 CARTON (0363-8201-19) > 113 g in 1 TUBE (0363-8201-12) |
NDC Code | 0363-8201-19 |
Proprietary Name | Walgreens |
Package Description | 1 TUBE in 1 CARTON (0363-8201-19) > 113 g in 1 TUBE (0363-8201-12) |
Product NDC | 0363-8201 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Fluoride |
Dosage Form Name | PASTE, DENTIFRICE |
Route Name | DENTAL |
Start Marketing Date | 20121001 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Walgreens |
Substance Name | SODIUM MONOFLUOROPHOSPHATE |
Strength Number | .76 |
Strength Unit | g/100g |
Pharmaceutical Classes |