Product NDC: | 50048-015 |
Proprietary Name: | ORAL ASSIST |
Non Proprietary Name: | ORAL ASSIST |
Active Ingredient(s): | 30; 12; 6; 12; 6; 6 [hp_C]/33.33mg; [hp_C]/33.33mg; [hp_X]/33.33mg; [hp_C]/33.33mg; [hp_C]/33.33mg; [hp_X]/33.33mg & nbsp; ORAL ASSIST |
Administration Route(s): | ORAL |
Dosage Form(s): | TINCTURE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50048-015 |
Labeler Name: | W LAST CC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20100101 |
Package NDC: | 50048-015-50 |
Package Description: | 100 mg in 1 BOTTLE, GLASS (50048-015-50) |
NDC Code | 50048-015-50 |
Proprietary Name | ORAL ASSIST |
Package Description | 100 mg in 1 BOTTLE, GLASS (50048-015-50) |
Product NDC | 50048-015 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ORAL ASSIST |
Dosage Form Name | TINCTURE |
Route Name | ORAL |
Start Marketing Date | 20100101 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | W LAST CC |
Substance Name | BELLADONNA LEAF; CALCIUM SULFIDE; FERROSOFERRIC PHOSPHATE; MERCURIUS SOLUBILIS; SALICYLIC ACID; SILICON DIOXIDE |
Strength Number | 30; 12; 6; 12; 6; 6 |
Strength Unit | [hp_C]/33.33mg; [hp_C]/33.33mg; [hp_X]/33.33mg; [hp_C]/33.33mg; [hp_C]/33.33mg; [hp_X]/33.33mg |
Pharmaceutical Classes |