FNG

Manufacturer
Deseret Biologicals, Inc. | Apotheca Company
Effective date
2016-12-09
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 01:21:09

Label at a glance#

ProductFNG
Active ingredientBERBERIS VULGARIS ROOT BARK, HORSERADISH, ECHINACEA ANGUSTIFOLIA, LOMATIUM DISSECTUM ROOT, MYRRH, TABEBUIA IMPETIGINOSA BARK, GOLDENSEAL, PROPOLIS WAX, FORMALDEHYDE, SUS SCROFA ADRENAL GLAND, SUS SCROFA THYMUS, IRON, IRIDIUM, LYCOPODIUM CLAVATUM SPORE, PHOSPHORIC ACID, PULSATILLA VULGARIS, SELENIUM, ZINC, ADENOSINE TRIPHOSPHATE DISODIUM, ALTERNARIA ALTERNATA, ASPERGILLUS NIGER VAR. NIGER, CANDIDA ALBICANS, CANDIDA PARAPSILOSIS, MUCOR RACEMOSUS, AUREOBASIDIUM PULLULANS VAR. PULLUTANS, RHIZOPUS STOLONIFER, SACCHAROMYCES CEREVISIAE, METHYLCOBALAMIN, LACTIC ACID, L-, STACHYBOTRYS CHARTARUM, ESCHERICHIA COLI, BRUGIA MALAYI
Label structure9 sections

Dosage and administration

1-10 drops under the tongue, 3 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

Berberis Vulgaris 3X, Cochlearia Armoracia 3X, Echinacea (Angustifolia) 3X, Lomatium Dissectum 3X, Myrrha 3X, Tabebuia Impetiginosa 3X, Hydrastis Canadensis 6X, Propolis 6X, Formalinum 6X, 12X, 30X, 12C, 30C, 200C, Glandula Suprarenalis Suis 8X, Thymus (Suis) 8X, Ferrum Metallicum 12X, Iridium Metallicum 12X, Lycopodium Clavatum 12X, Phosphoricum Acidum 12X, Pulsatilla (Vulgaris) 12X, Selenium Metallicum 12X, Zincum Metallicum 12X, Adenosinum Triphosphoricum Dinatrum 12X, 30X, 200X, Alternaria Tenuis Nees 12X, 30X, 200X, Aspergillus Niger 12X, 30X, 200X, Candida Albicans 12X, 30X, 200X, Candida Parapsilosis 12X, 30X, 200X, Mucor Racemosus 12X, 30X, 200X, Pullularia Pullulans 12X, 30X, 200X, Rhizopus Nigricans 12X, 30X, 200X, Torula Cerevisiae 12X, 30X, 200X, Methylcobalamin 12X, 30X, 200X, Sarcolacticum Acidum 12X, 30X, 200X, Stachybotrys Chartarum 12X, 30X, 200X, Mutabile Bacillus (Bach) 30C, Brugia Malayi 39C, 60C, 200C.

HOMEOPATHIC INDICATIONS:

OTC - PURPOSE SECTION

For temporary relief of symptoms related to yeast, including gastritis, constipation, mucous congestion, abdominal gas, headaches, fatigue, alcohol cravings, anxiety, vaginitis, rectal itching, cravings for sweets, foggy brain, hyperactivity, mood swings, diarrhea and dizziness.**


**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 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 a physician or a Poison Control Center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

1-10 drops under the tongue, 3 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 temporary relief of symptoms related to yeast, including gastritis, constipation, mucous congestion, abdominal gas, headaches, fatigue, alcohol cravings, anxiety, vaginitis, rectal itching, cravings for sweets, foggy brain, hyperactivity, mood swings, diarrhea and dizziness.**


**These statements are based upon 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

**For a complete list of Fungus Nosodes contact Deseret Biologicals, Inc.

PACKAGE DISPLAY LABEL:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DESBIO

NDC 43742-0672-1

HOMEOPATHIC

FNG

1 FL OZ (30 ml)

FNGFNG

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43742-074343742-0743-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 34 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
261ed9e2-4580-41f7-9744-d885f5e8bac36b0f3cf2-8982-4b57-a4e5-a009cac9c92f2016-12-09WarningsExact identifier
spl id: 261ed9e2-4580-41f7-9744-d885f5e8bac3
spl set id: 6b0f3cf2-8982-4b57-a4e5-a009cac9c92f

Reported adverse events (FAERS/openFDA)#

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