NDC 43742-1568 – Energize

Lactic Acid, L- 3 [hp_X]/mL; Viscum Album Fruiting Top 3 [hp_X]/mL; Iodine 3 [hp_X]/mL; Fucus Vesiculosus 6 [hp_X]/mL; Galium Aparine Whole 6 [hp_X]/mL; Sodium… · Liquid · Oral

Human Otc Drug

Product NDC43742-1568

Product details

Brand name
Energize
Generic name
Sarcolacticum Acidum, Viscum Album, Iodium, Fucus Vesiculosus, Galium Aparine, Natrum Oxalaceticum, Thyroidinum (Suis), DHEA (Dehydroepiandrosterone), Phenyl Isothiocyanate, Tri-Iodothyronine, Tyramine, Adenosinum Triphosphoricum Dinatrum, alpha-Ketoglutaricum Acidum, Fumaricum Acidum, Malic Acid, Colchicum Autumnale, Conium Maculatum, Funiculus Umbilicalis Suis, Hepar Suis, Medulla Ossis Suis, Pineal Gland (Suis), Spleen (Suis), Thymus (Suis), Calcarea Fluorica, Pulsatilla (Vulgaris), Spongia T
Labeler
Deseret Biologicals, Inc.
Dosage form
Liquid
Route
Oral
Marketing category
UNAPPROVED HOMEOPATHIC
Marketed since
October 2, 2019
Listing expires
December 31, 2026
Pharmacologic class
Corticosteroid; l-Triiodothyronine

Active ingredients

Uses, dosage, side effects and warnings for Energize →

Package NDC codes (1)

Package NDCDescriptionSince
43742-1568-130 mL in 1 BOTTLE, DROPPER (43742-1568-1)Oct 2, 2019

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