Product NDC: | 44946-1036 |
Proprietary Name: | Tri-Vitamin with Fluoride |
Non Proprietary Name: | Vitamin A, Ascorbic Acid, Vitamin D, and Sodium Fluoride |
Active Ingredient(s): | 35; .5; 1500; 400 mg/mL; mg/mL; [iU]/mL; [iU]/mL & nbsp; Vitamin A, Ascorbic Acid, Vitamin D, and Sodium Fluoride |
Administration Route(s): | ORAL |
Dosage Form(s): | SOLUTION/ DROPS |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 44946-1036 |
Labeler Name: | Sancilio & Company Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20111220 |
Package NDC: | 44946-1036-8 |
Package Description: | 50 mL in 1 BOTTLE, PLASTIC (44946-1036-8) |
NDC Code | 44946-1036-8 |
Proprietary Name | Tri-Vitamin with Fluoride |
Package Description | 50 mL in 1 BOTTLE, PLASTIC (44946-1036-8) |
Product NDC | 44946-1036 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Vitamin A, Ascorbic Acid, Vitamin D, and Sodium Fluoride |
Dosage Form Name | SOLUTION/ DROPS |
Route Name | ORAL |
Start Marketing Date | 20111220 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Sancilio & Company Inc |
Substance Name | ASCORBIC ACID; SODIUM FLUORIDE; VITAMIN A; VITAMIN D |
Strength Number | 35; .5; 1500; 400 |
Strength Unit | mg/mL; mg/mL; [iU]/mL; [iU]/mL |
Pharmaceutical Classes | Vitamin A [Chemical/Ingredient],Vitamin A [EPC] |