Product NDC: | 53499-1390 |
Proprietary Name: | ALPHA SH |
Non Proprietary Name: | SANGUINARIA CANADENSIS ROOT, GOLDENSEAL, SILICON DIOXIDE, POTASSIUM CHLORIDE, PULSATILLA VULGARIS |
Active Ingredient(s): | 6; 3; 3; 6; 6 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 & nbsp; SANGUINARIA CANADENSIS ROOT, GOLDENSEAL, SILICON DIOXIDE, POTASSIUM CHLORIDE, PULSATILLA VULGARIS |
Administration Route(s): | SUBLINGUAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 53499-1390 |
Labeler Name: | Nature's Way Products, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20110818 |
Package NDC: | 53499-1390-1 |
Package Description: | 4 BLISTER PACK in 1 BOX (53499-1390-1) > 10 TABLET in 1 BLISTER PACK |
NDC Code | 53499-1390-1 |
Proprietary Name | ALPHA SH |
Package Description | 4 BLISTER PACK in 1 BOX (53499-1390-1) > 10 TABLET in 1 BLISTER PACK |
Product NDC | 53499-1390 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | SANGUINARIA CANADENSIS ROOT, GOLDENSEAL, SILICON DIOXIDE, POTASSIUM CHLORIDE, PULSATILLA VULGARIS |
Dosage Form Name | TABLET |
Route Name | SUBLINGUAL |
Start Marketing Date | 20110818 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Nature's Way Products, Inc. |
Substance Name | GOLDENSEAL; POTASSIUM CHLORIDE; PULSATILLA VULGARIS; SANGUINARIA CANADENSIS ROOT; SILICON DIOXIDE |
Strength Number | 6; 3; 3; 6; 6 |
Strength Unit | [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 |
Pharmaceutical Classes |