Energise RxS

Product NDC

43742-0026

11-digit product format

437420026

Labeler code

43742

Product ID

43742-0026_d8fc6dd7-d91d-4054-8632-a4819c4451f0

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

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

Dosage form

TABLET

Route

ORAL

Labeler

Deseret Biologicals

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

2012-09-26

Marketing end

2022-10-28

Substance

.ALPHA.-KETOGLUTARIC ACID; ADENOSINE TRIPHOSPHATE; CALCIUM FLUORIDE; COLCHICUM AUTUMNALE BULB; CONIUM MACULATUM FLOWERING TOP; CORTISONE ACETATE; ESCHERICHIA COLI; FUCUS VESICULOSUS; FUMARIC ACID; GALIUM APARINE; IODINE; LACTIC ACID, L-; LIOTHYRONINE; MALIC ACID; MERCURIC CHLORIDE; PHENYL ISOTHIOCYANATE; PORK LIVER; PRASTERONE; PULSATILLA VULGARIS; SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS; SODIUM DIETHYL OXALACETATE; SPONGIA OFFICINALIS SKELETON, ROASTED; SUS SCROFA BONE MARROW; SUS SCROFA PINEAL GLAND; SUS SCROFA SPLEEN; SUS SCROFA THYMUS; SUS SCROFA UMBILICAL CORD; THYROID, PORCINE; TYRAMINE; VISCUM ALBUM FRUITING TOP

Active strength

7 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_C]/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_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

Pharmacologic classes

Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC], Triiodothyronine [CS], l-Triiodothyronine [EPC]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record