| Product NDC: | 55918-002 |
| Proprietary Name: | Phocal pHn |
| Non Proprietary Name: | Sodium Fluoride |
| Active Ingredient(s): | .055 mg/1 & nbsp; Sodium Fluoride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | DISC |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 55918-002 |
| 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: | 55918-002-20 |
| Package Description: | 2 BLISTER PACK in 1 BOX (55918-002-20) > 10 DISC in 1 BLISTER PACK |
| NDC Code | 55918-002-20 |
| Proprietary Name | Phocal pHn |
| Package Description | 2 BLISTER PACK in 1 BOX (55918-002-20) > 10 DISC in 1 BLISTER PACK |
| Product NDC | 55918-002 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sodium Fluoride |
| 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 | SODIUM FLUORIDE |
| Strength Number | .055 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |