Product NDC: | 54973-2957 |
Proprietary Name: | PMS |
Non Proprietary Name: | VIBURNUM OPULUS BARK, CAULOPHYLLUM THALICTROIDES ROOT, ANAMIRTA COCCULUS SEED, and GELSEMIUM SEMPERVIRENS ROOT |
Active Ingredient(s): | 3; 3; 3; 2 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 & nbsp; VIBURNUM OPULUS BARK, CAULOPHYLLUM THALICTROIDES ROOT, ANAMIRTA COCCULUS SEED, and GELSEMIUM SEMPERVIRENS ROOT |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, SOLUBLE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54973-2957 |
Labeler Name: | Hyland's |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 19970926 |
Package NDC: | 54973-2957-1 |
Package Description: | 50 TABLET, SOLUBLE in 1 BOTTLE, PLASTIC (54973-2957-1) |
NDC Code | 54973-2957-1 |
Proprietary Name | PMS |
Package Description | 50 TABLET, SOLUBLE in 1 BOTTLE, PLASTIC (54973-2957-1) |
Product NDC | 54973-2957 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | VIBURNUM OPULUS BARK, CAULOPHYLLUM THALICTROIDES ROOT, ANAMIRTA COCCULUS SEED, and GELSEMIUM SEMPERVIRENS ROOT |
Dosage Form Name | TABLET, SOLUBLE |
Route Name | ORAL |
Start Marketing Date | 19970926 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Hyland's |
Substance Name | ANAMIRTA COCCULUS SEED; CAULOPHYLLUM THALICTROIDES ROOT; GELSEMIUM SEMPERVIRENS ROOT; VIBURNUM OPULUS BARK |
Strength Number | 3; 3; 3; 2 |
Strength Unit | [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 |
Pharmaceutical Classes |