NDC 43742-0026

Energise RxS

Sarcolacticum Acidum, Viscum Album, Iodium, Colchicum Atumnale, Conium Maculatum, Fucus Vesiculosus, Galiu Aparine, Natrum Oxalaceticum

Energise RxS is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Deseret Biologicals. The primary component is Lactic Acid, L-; Viscum Album Fruiting Top; Iodine; Colchicum Autumnale Bulb; Conium Maculatum Flowering Top; Fucus Vesiculosus; Galium Aparine; Sodium Diethyl Oxalacetate; Thyroid, Porcine; Prasterone; Phenyl Isothiocyanate; Liothyronine; Tyramine; .alpha.-ketoglutaric Acid; Adenosine Triphosphate; Fumaric Acid; Malic Acid; Sus Scrofa Umbilical Cord; Pork Liver; Sus Scrofa Bone Marrow; Sus Scrofa Pineal Gland; Sus Scrofa Spleen; Sus Scrofa Thymus; Calcium Fluoride; Pulsatilla Vulgaris; Spongia Officinalis Skeleton, Roasted; Cortisone Acetate; Mercuric Chloride; Salmonella Enterica Subsp. Enterica Serovar Enteritidis; Escherichia Coli.

Product ID43742-0026_6300af6c-0aa4-41c8-ac60-11e0f51cf57f
NDC43742-0026
Product TypeHuman Prescription Drug
Proprietary NameEnergise RxS
Generic NameSarcolacticum Acidum, Viscum Album, Iodium, Colchicum Atumnale, Conium Maculatum, Fucus Vesiculosus, Galiu Aparine, Natrum Oxalaceticum
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2012-09-26
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameDeseret Biologicals
Substance NameLACTIC ACID, L-; VISCUM ALBUM FRUITING TOP; IODINE; COLCHICUM AUTUMNALE BULB; CONIUM MACULATUM FLOWERING TOP; FUCUS VESICULOSUS; GALIUM APARINE; SODIUM DIETHYL OXALACETATE; THYROID, PORCINE; PRASTERONE; PHENYL ISOTHIOCYANATE; LIOTHYRONINE; TYRAMINE; .ALPHA.-KETOGLUTARIC ACID; ADENOSINE TRIPHOSPHATE; FUMARIC ACID; MALIC ACID; SUS SCROFA UMBILICAL CORD; PORK LIVER; SUS SCROFA BONE MARROW; SUS SCROFA PINEAL GLAND; SUS SCROFA SPLEEN; SUS SCROFA THYMUS; CALCIUM FLUORIDE; PULSATILLA VULGARIS; SPONGIA OFFICINALIS SKELETON, ROASTED; CORTISONE ACETATE; MERCURIC CHLORIDE; SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS; ESCHERICHIA COLI
Active Ingredient Strength3 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_C]/1; [hp_C]/1
Pharm Classesl-Triiodothyronine [EPC],Triiodothyronine [CS],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 43742-0026-1

60 TABLET in 1 BOTTLE (43742-0026-1)
Marketing Start Date2012-09-26
Marketing End Date2022-10-28
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 43742-0026-1 [43742002601]

Energise RxS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-09-26
Inactivation Date2020-01-31

Drug Details


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