Product NDC: | 53499-0339 |
Proprietary Name: | ALPHA CF |
Non Proprietary Name: | ACONITUM NAPELLUS, BRYONIA ALBA ROOT, EUCALYPTUS GLOBULUS LEAF, EUPATORIUM PERFOLIATUM FLOWERING TOP, GELSEMIUM SEMPERVIRENS ROOT,IPECAC , PHOSPHORUS |
Active Ingredient(s): | 4; 4; 2; 2; 4; 3; 6 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 & nbsp; ACONITUM NAPELLUS, BRYONIA ALBA ROOT, EUCALYPTUS GLOBULUS LEAF, EUPATORIUM PERFOLIATUM FLOWERING TOP, GELSEMIUM SEMPERVIRENS ROOT,IPECAC , PHOSPHORUS |
Administration Route(s): | SUBLINGUAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 53499-0339 |
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: | 53499-0339-2 |
Package Description: | 1 BOTTLE, GLASS in 1 BOX (53499-0339-2) > 120 TABLET in 1 BOTTLE, GLASS |
NDC Code | 53499-0339-2 |
Proprietary Name | ALPHA CF |
Package Description | 1 BOTTLE, GLASS in 1 BOX (53499-0339-2) > 120 TABLET in 1 BOTTLE, GLASS |
Product NDC | 53499-0339 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ACONITUM NAPELLUS, BRYONIA ALBA ROOT, EUCALYPTUS GLOBULUS LEAF, EUPATORIUM PERFOLIATUM FLOWERING TOP, GELSEMIUM SEMPERVIRENS ROOT,IPECAC , PHOSPHORUS |
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 | ACONITUM NAPELLUS; BRYONIA ALBA ROOT; EUCALYPTUS GLOBULUS LEAF; EUPATORIUM PERFOLIATUM FLOWERING TOP; GELSEMIUM SEMPERVIRENS ROOT; IPECAC; PHOSPHORUS |
Strength Number | 4; 4; 2; 2; 4; 3; 6 |
Strength Unit | [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 |
Pharmaceutical Classes |