| Product NDC: | 51206-305 |
| Proprietary Name: | Xylishield |
| Non Proprietary Name: | Sodium Fluoride |
| Active Ingredient(s): | .3325 g/133g & nbsp; Sodium Fluoride |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | PASTE, DENTIFRICE |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 51206-305 |
| Labeler Name: | Ultradent Products, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part355 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20101027 |
| Package NDC: | 51206-305-08 |
| Package Description: | 1 TUBE in 1 BOX (51206-305-08) > 133 g in 1 TUBE |
| NDC Code | 51206-305-08 |
| Proprietary Name | Xylishield |
| Package Description | 1 TUBE in 1 BOX (51206-305-08) > 133 g in 1 TUBE |
| Product NDC | 51206-305 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Sodium Fluoride |
| Dosage Form Name | PASTE, DENTIFRICE |
| Route Name | DENTAL |
| Start Marketing Date | 20101027 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Ultradent Products, Inc. |
| Substance Name | SODIUM FLUORIDE |
| Strength Number | .3325 |
| Strength Unit | g/133g |
| Pharmaceutical Classes |