| 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 |