| NDC Code: |
50114-7055 |
| Proprietary Name: |
Placenta Compositum |
| Suffix: |
|
| Non-Proprietary Name: |
HORSE CHESTNUT and LACTIC ACID, L- and CLAVICEPS PURPUREA SCLEROTIUM and CUPRIC SULFATE and MELILOTUS OFFICINALIS TOP and SUS SCROFA PLACENTA and SOLANUM NIGRUM WHOLE and STROPHANTHUS HISPIDUS SEED and SUS SCROFA EMBRYO and SODIUM PYRUVATE and SUS SCROFA VEIN and SUS SCROFA ARTERY and SUS SCROFA UMBILICAL CORD and TOBACCO LEAF and VIPERA BERUS VENOM and BARIUM CARBONATE and LEAD IODIDE |
| Dosage Form: |
INJECTION |
| Method: |
INTRADERMAL; INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
| Original Marketing Date: |
30-04-2009 |
| Category Name: |
UNAPPROVED HOMEOPATHIC |
| Application Number: |
|
| Labeler: |
HEEL INC |
| Substance Name: |
BARIUM CARBONATE; CLAVICEPS PURPUREA SCLEROTIUM; CUPRIC SULFATE; HORSE CHESTNUT; LACTIC ACID, L-; LEAD IODIDE; MELILOTUS OFFICINALIS TOP; SODIUM PYRUVATE; SOLANUM NIGRUM WHOLE; STROPHANTHUS HISPIDUS SEED; SUS SCROFA ARTERY; SUS SCROFA EMBRYO; SUS SCROFA PLACENTA; SUS SCROFA UMBILICAL CORD; SUS SCROFA VEIN; TOBACCO LEAF; VIPERA BERUS VENOM |
| Active Numerator Strength: |
13; 4; 6; 4; 4; 18; 6; 8; 6; 6; 10; 8; 6; 10; 8; 10; 10 |
| Active Ingredient Unit: |
[hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL |
| Pharm Classes: |
Non-Standardized Plant Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Allergens [Chemical/Ingredient],Plant Proteins [Chemical/Ingredient] |
| DEA Schedule: |
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