NDC 57955-3001

Sciatiplex

Aesculus Hippocastanum, Ammonium Muriaticum, Arsenicum Album, Belladonna, Capsicum Annuum, Causticum, Colchicum Autumnale, Colocynthis, Gnaphalium Polycephalum, Hypericum, Ignatia Amara, Kalmia, Magnesia Phosphorica, Rhus Tox, Ruta.

Sciatiplex is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by King Bio Inc.. The primary component is Ammonium Chloride; Arsenic Trioxide; Atropa Belladonna; Capsicum; Causticum; Citrullus Colocynthis Fruit Pulp; Colchicum Autumnale Bulb; Horse Chestnut; Hypericum Perforatum Whole; Kalmia Latifolia Leaf; Magnesium Phosphate, Dibasic Trihydrate; Pseudognaphalium Obtusifolium Whole; Ruta Graveolens Flowering Top; Strychnos Ignatii Seed; Toxicodendron Pubescens Leaf.

Product ID57955-3001_00f8f02d-132c-4912-b65b-5878fa603e1d
NDC57955-3001
Product TypeHuman Otc Drug
Proprietary NameSciatiplex
Generic NameAesculus Hippocastanum, Ammonium Muriaticum, Arsenicum Album, Belladonna, Capsicum Annuum, Causticum, Colchicum Autumnale, Colocynthis, Gnaphalium Polycephalum, Hypericum, Ignatia Amara, Kalmia, Magnesia Phosphorica, Rhus Tox, Ruta.
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2022-02-01
Marketing CategoryUNAPPROVED HOMEOPATHIC /
Labeler NameKing Bio Inc.
Substance NameAMMONIUM CHLORIDE; ARSENIC TRIOXIDE; ATROPA BELLADONNA; CAPSICUM; CAUSTICUM; CITRULLUS COLOCYNTHIS FRUIT PULP; COLCHICUM AUTUMNALE BULB; HORSE CHESTNUT; HYPERICUM PERFORATUM WHOLE; KALMIA LATIFOLIA LEAF; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; PSEUDOGNAPHALIUM OBTUSIFOLIUM WHOLE; RUTA GRAVEOLENS FLOWERING TOP; STRYCHNOS IGNATII SEED; TOXICODENDRON PUBESCENS LEAF
Active Ingredient Strength10 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
Pharm ClassesAllergens [CS], Calculi Dissolution Agent [EPC], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Osmotic Activity [MoA], Osmotic Laxative [EPC], Plant Proteins [CS], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE], Vegetable Proteins [CS]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 57955-3001-2

59 mL in 1 BOTTLE, SPRAY (57955-3001-2)
Marketing Start Date2022-02-01
NDC Exclude FlagN
Sample Package?N

Drug Details


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