Energize

Manufacturer
Deseret Biologicals | Apotheca Company
Effective date
2018-10-30
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 00:47:43

Label at a glance#

ProductEnergize
Active ingredientLACTIC ACID, L-, VISCUM ALBUM FRUITING TOP, IODINE, COLCHICUM AUTUMNALE BULB, CONIUM MACULATUM FLOWERING TOP, FUCUS VESICULOSUS, GALIUM APARINE, SUS SCROFA THYROID, PRASTERONE, PHENYL ISOTHIOCYANATE, TYRAMINE, ADENOSINE TRIPHOSPHATE DISODIUM, OXOGLURIC ACID, FUMARIC ACID, MALIC ACID, SODIUM DIETHYL OXALACETATE, SUS SCROFA UMBILICAL CORD, PORK LIVER, SUS SCROFA BONE MARROW, SUS SCROFA PINEAL GLAND, SUS SCROFA SPLEEN, SUS SCROFA THYMUS, CALCIUM FLUORIDE, ANEMONE PULSATILLA, SPONGIA OFFICINALIS SKELETON, ROASTED, CORTISONE ACETATE, MERCURIC CHLORIDE, LIOTHYRONINE, SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS, ESCHERICHIA COLI
Label structure9 sections

Dosage and administration

One tablet three times daily or as directed by a health professional. 

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Sarcolacticum Acidum 3X, Viscum Album 3X, Iodium 3X, 6X, 12X, 30X, Colchicum Autumnale 6X, Conium Maculatum 6X, Fucus Vesiculosus 6X, Galium Aparine 6X, Thyroidinum (Suis) 6X, 12X, 30X, DHEA (Dehydroepiandrosterone) 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Phenyl Isothiocyanate 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Tyramine 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Adenosinum Triphosphoricum Dinatrum 7X, Alpha-Ketoglutaricum Acidum 7X, Fumaricum Acidum 7X, Malic Acidum 7X, Natrum Oxalaceticum 8X, Funiculus Umbilicalis Suis 8X, 12X, 30X, Hepar Suis 8X, 12X, 30X, Medulla Ossis Suis 8X, 12X, 30X, Pineal Gland (Suis) 8X, 12X, 30X, Spleen (Suis) 8X, 12X, 30X, Thymus (Suis) 8X, 12X, 30X, Calcarea Fluorica 12X, Pulsatilla (Vulgaris) 12X, Spongia Tosta 12X, Cortisone Aceticum 30X, Mercurius Corrosivus 60X, 100X, 200X, Tri-Iodothyronine 6X, 12X, 30X, 200X, 15C, 30C, 60C, 200C, Gaertner Bacillus (Bach) 30C, Mutabile Bacillus (Bach) 30C.

HOMEOPATHIC INDICATIONS:

OTC - PURPOSE SECTION

For temporary relief of symptoms related to the thyroid system.**

**These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

WARNINGS:

WARNINGS SECTION

Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away.

If pregnant or breast-feeding, ask a health professional before use.

Tamper seal: "Sealed for Your Protection." Do not use if seal is broken or missing.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

One tablet three times daily or as directed by a health professional. 

HOMEOPATHIC INDICATIONS:

INDICATIONS & USAGE SECTION

For temporary relief of symptoms related to the thyroid system.**

**These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Lactose, Magnesium Stearate, Microcrystalline Cellulose.

QUESTIONS:

OTC - QUESTIONS SECTION

Dist. by Deseret Biologicals, Inc.

469 W. Parkland Drive

Sandy, UT 84070   www.desbio.com

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DESBIO

NDC 43742-0724-1

HOMEOPATHIC

ENERGIZE

90 TABLETS

EnergizeEnergize

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 2 · 41 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43742-072443742-0724-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 33 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
f05f836a-9510-4dbc-bb3c-83c7617a9c7b54e8f581-9286-4784-bd48-68f8a2e5eba42018-10-30WarningsExact identifier
spl id: f05f836a-9510-4dbc-bb3c-83c7617a9c7b
spl set id: 54e8f581-9286-4784-bd48-68f8a2e5eba4

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.