Eczema Skin Care (Newton Laboratories, Inc.)
Welcome to the PulseAid listing for the Eczema Skin Care drug offered from Newton Laboratories, Inc.. This Calcium [Chemical/Ingredient],Calcium [EPC],Phosphate Binder [EPC],Phosphate Chelating Activity [MoA],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],Seed Storage Proteins [Chemical/Ingredient] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
LABELER NAME / MANUFACTURER: | Newton Laboratories, Inc. |
NON-PROPRIETARY NAME: | Antimon. crud., Arsenicum alb., Berber. vulg., Bovista , Bryonia , Cantharis , Chelidonium majus, Croton, Dulcamara, Graphites, Hepar sulph. calc., Lycopodium Mezereum, Nux vom, Petroleum, Pulex irrit |
SUBSTANCE NAME: | ANTIMONY TRISULFIDE; ARSENIC TRIOXIDE; BERBERIS VULGARIS ROOT BARK; GIANT PUFFBALL; BRYONIA ALBA ROOT; LYTTA VESICATORIA; CHELIDONIUM MAJUS; CROTON TIGLIUM SEED; SOLANUM DULCAMARA TOP; GRAPHITE; CALCI |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Calcium [Chemical/Ingredient],Calcium [EPC],Phosphate Binder [EPC],Phosphate Chelating Activity [MoA],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],Seed Storage Proteins [Chemical/Ingredient] |
ROUTE: | ORAL |
DOSAGE FORM: | LIQUID |
MARKETING CATEGORY NAME: | UNAPPROVED HOMEOPATHIC |
START MARKETING DATE: | 2011-06-01 |
END MARKETING DATE: | 0000-00-00 |
Eczema Skin Care HUMAN PRESCRIPTION DRUG Details:
Item Description | Eczema Skin Care from Newton Laboratories, Inc. |
LABELER NAME: | Newton Laboratories, Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 20; 20; 20; 20; 20; 20; 20; 20; 20; 20; 20; 20; 20; 20; 20; 20; 20; 20; 20; 20; 20; 8; 8; 8; 8; 3; 3; 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; [h) |
START MARKETING DATE: | 2011-06-01 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 55714-4402_3cbecb6e-2002-8de8-bee3-c612623eb03c |
PRODUCT NDC: | 55714-4402 |
APPLICATION NUMBER: | |
Other ANTIMONY TRISULFIDE; ARSENIC TRIOXIDE; BERBERIS VULGARIS ROOT BARK; GIANT PUFFBALL; BRYONIA ALBA ROOT; LYTTA VESICATORIA; CHELIDONIUM MAJUS; CROTON TIGLIUM SEED; SOLANUM DULCAMARA TOP; GRAPHITE; CALCI Pharmaceutical Manufacturers / Labelers: