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Psoriaforce
Psoriaforce - 57520-0957-1 - (Baptisia tinctoria, Berberis vulgaris, Echinacea, Glycyrrhiza glabra, Hydrastis canadensis, Lappa major, Phytolacca decandra, Rhamnus frangula Lappa major, Phytolacca decandra, Rhamnus frangula, Rhamn)
Drug Information of Psoriaforce
| Product NDC: | 57520-0957 |
| Proprietary Name: | Psoriaforce |
| Non Proprietary Name: | Baptisia tinctoria, Berberis vulgaris, Echinacea, Glycyrrhiza glabra, Hydrastis canadensis, Lappa major, Phytolacca decandra, Rhamnus frangula Lappa major, Phytolacca decandra, Rhamnus frangula, Rhamn |
| Active Ingredient(s): | 3; 12; 3; 3; 12; 12; 3; 3; 3; 3; 3; 12; 12; 12; 3; 12; 12; 12; 3; 3 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL & nbsp; Baptisia tinctoria, Berberis vulgaris, Echinacea, Glycyrrhiza glabra, Hydrastis canadensis, Lappa major, Phytolacca decandra, Rhamnus frangula Lappa major, Phytolacca decandra, Rhamnus frangula, Rhamn |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Psoriaforce
| Product NDC: | 57520-0957 |
| Labeler Name: | Apotheca Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20111114 |
Package Information of Psoriaforce
| Package NDC: | 57520-0957-1 |
| Package Description: | 30 mL in 1 BOTTLE, DROPPER (57520-0957-1) |
NDC Information of Psoriaforce
| NDC Code | 57520-0957-1 |
| Proprietary Name | Psoriaforce |
| Package Description | 30 mL in 1 BOTTLE, DROPPER (57520-0957-1) |
| Product NDC | 57520-0957 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Baptisia tinctoria, Berberis vulgaris, Echinacea, Glycyrrhiza glabra, Hydrastis canadensis, Lappa major, Phytolacca decandra, Rhamnus frangula Lappa major, Phytolacca decandra, Rhamnus frangula, Rhamn |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20111114 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Apotheca Company |
| Substance Name | ARCTIUM LAPPA ROOT; ARSENIC TRIIODIDE; BAPTISIA TINCTORIA ROOT; BERBERIS VULGARIS ROOT BARK; CLEMATIS RECTA FLOWERING TOP; DAPHNE MEZEREUM BARK; ECHINACEA, UNSPECIFIED; FRANGULA ALNUS BARK; FRANGULA PURSHIANA BARK; GLYCYRRHIZA GLABRA; GOLDENSEAL; GRAPHITE; KEROSENE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PHYTOLACCA AMERICANA ROOT; POTASSIUM CHLORIDE; POTASSIUM SULFATE; SEPIA OFFICINALIS JUICE; TRIFOLIUM PRATENSE FLOWER; ZANTHOXYLUM AMERICANUM BARK |
| Strength Number | 3; 12; 3; 3; 12; 12; 3; 3; 3; 3; 3; 12; 12; 12; 3; 12; 12; 12; 3; 3 |
| Strength Unit | [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL |
| Pharmaceutical Classes |
