Product NDC: | 55918-001 |
Proprietary Name: | Phocal Apf |
Non Proprietary Name: | Sodium Fluoride, hydrofluoric acid |
Active Ingredient(s): | .0094; .0466 mg/1; mg/1 & nbsp; Sodium Fluoride, hydrofluoric acid |
Administration Route(s): | TOPICAL |
Dosage Form(s): | DISC |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55918-001 |
Labeler Name: | U.S.I.A. Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20130101 |
Package NDC: | 55918-001-20 |
Package Description: | 2 BLISTER PACK in 1 BOX (55918-001-20) > 10 DISC in 1 BLISTER PACK |
NDC Code | 55918-001-20 |
Proprietary Name | Phocal Apf |
Package Description | 2 BLISTER PACK in 1 BOX (55918-001-20) > 10 DISC in 1 BLISTER PACK |
Product NDC | 55918-001 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Sodium Fluoride, hydrofluoric acid |
Dosage Form Name | DISC |
Route Name | TOPICAL |
Start Marketing Date | 20130101 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | U.S.I.A. Inc |
Substance Name | HYDROFLUORIC ACID; SODIUM FLUORIDE |
Strength Number | .0094; .0466 |
Strength Unit | mg/1; mg/1 |
Pharmaceutical Classes |