Bio Co-Enzyme Phase

Manufacturer
Deseret Biologicals, Inc. | Apotheca Company
Effective date
2021-08-05
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:38:57

Label at a glance#

ProductBio Co-Enzyme Phase
Active ingredientBETA VULGARIS, ASCORBIC ACID, CYSTEINE, SODIUM DIETHYL OXALACETATE, NIACINAMIDE, ANEMONE PULSATILLA, PYRIDOXINE HYDROCHLORIDE, RIBOFLAVIN, THIAMINE HYDROCHLORIDE, ACONITIC ACID, (Z)-, OXOGLURIC ACID, THIOCTIC ACID, CEROUS OXALATE NONAHYDRATE, ANHYDROUS CITRIC ACID, FUMARIC ACID, MAGNESIUM OROTATE DIHYDRATE, MALIC ACID, NADIDE, SODIUM PYRUVATE, PANTOTHENIC ACID, SUCCINIC ACID, EPINEPHRINE, ADENOSINE TRIPHOSPHATE DISODIUM, CALCIUM SULFIDE, SULFUR, MANGANESE PHOSPHATE, DIBASIC, BARIUM OXALOSUCCINATE, PROTEUS MORGANII
Label structure9 sections

Dosage and administration

1-10 drops under the tongue, 2 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Beta Vulgaris 4X, Ascorbicum Acidum 6X, Cysteinum 6X, Natrum Oxalaceticum 6X, Nicotinamidum 6X, Pulsatilla (Vulgaris) 6X, Pyridoxinum Hydrochloricum 6X, Riboflavinum 6X, Thiaminum Hydrochloricum 6X, Aconiticum Acidum, Cis 8X, alpha-Ketoglutaricum Acidum 8X, alpha-Lipoicum Acidum 8X, Cerium Oxalicum 8X, Citricum Acidum 6X, Fumaricum Acidum 8X, Magnesium Oroticum Dihydricum 8X, Malicum Acidum 8X, Nadidum 8X, Natrum Pyruvicum 8X, Pantothenic Acid 8X, Succinicum Acidum 8X, Adrenalinum 8X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Adenosinum Triphosphoricum Dinatrum 10X, Hepar Sulphuris Calcareum 10X, Sulphur 10X, Manganum Phosphoricum 16X, Barium Oxalsuccinicum 30C, Proteus (Morgani) 34C.

HOMEOPATHIC INDICATIONS:

OTC - PURPOSE SECTION

For the temporary relief of exhaustion, fatigue, and feelings of low energy.**

**These statements are based upon traditional 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 physician or a 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 physician or a Poison Control Center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

1-10 drops under the tongue, 2 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

HOMEOPATHIC INDICATIONS:

INDICATIONS & USAGE SECTION

For the temporary relief of exhaustion, fatigue, and feelings of low energy.**

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

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized Water, 25% Ethanol

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 43742-1254-1
HOMEOPATHIC
BIO CO-ENZYME PHASE
1 FL OZ (30 ml)

Bio Co-Enzyme PhaseBio Co-Enzyme Phase

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43742-125443742-1254-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 30 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
c9db2466-671a-4502-93a8-394d787cdb8ccaf111c7-e027-4d94-a4ae-a19227f32dc92021-08-05WarningsExact identifier
spl id: c9db2466-671a-4502-93a8-394d787cdb8c
spl set id: caf111c7-e027-4d94-a4ae-a19227f32dc9

Reported adverse events (FAERS/openFDA)#

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