| NDC Code: |
59088-109 |
| Proprietary Name: |
Multivitamin with Fluoride |
| Suffix: |
|
| Non-Proprietary Name: |
Sodium Fluoride |
| Dosage Form: |
TABLET, CHEWABLE |
| Method: |
ORAL |
| Original Marketing Date: |
01-06-2011 |
| Category Name: |
UNAPPROVED DRUG OTHER |
| Application Number: |
|
| Labeler: |
PURETEK CORPORATION |
| Substance Name: |
.ALPHA.-TOCOPHEROL ACETATE, DL-; ASCORBIC ACID; CHOLECALCIFEROL; CYANOCOBALAMIN; FOLIC ACID; NIACINAMIDE; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; SODIUM ASCORBATE; SODIUM FLUORIDE; THIAMINE MONONITRATE; VITAMIN A |
| Active Numerator Strength: |
15; 24; 400; 4.5; 300; 13.5; 1.05; 1.2; 36; 1; 1.05; 2500 |
| Active Ingredient Unit: |
[iU]/1; mg/1; [iU]/1; ug/1; ug/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; [iU]/1 |
| Pharm Classes: |
Vitamin A [Chemical/Ingredient],Vitamin A [EPC],Vitamin D [Chemical/Ingredient],Vitamin D [EPC],Vitamin B 12 [Chemical/Ingredient],Vitamin B12 [EPC] |
| DEA Schedule: |
|
