FDA.reportPublic FDA data

FNG

Manufacturer
Deseret Biologicals, Inc. | Apotheca Company
Effective date
2022-09-12
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:53:54

Label at a glance#

ProductFNG
Active ingredientBERBERIS VULGARIS ROOT BARK, HORSERADISH, ECHINACEA ANGUSTIFOLIA, LOMATIUM DISSECTUM ROOT, MYRRH, GOLDENSEAL, PROPOLIS WAX, SUS SCROFA ADRENAL GLAND, TABEBUIA IMPETIGINOSA BARK, SUS SCROFA THYMUS, FORMALDEHYDE, IRON, IRIDIUM, LYCOPODIUM CLAVATUM SPORE, PHOSPHORIC ACID, ANEMONE PULSATILLA, 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, Hydrastis Canadensis 6X, Propolis 6X, Glandula Suprarenalis Suis 8X, Tabebuia Impetiginosa 8X, Thymus (Suis) 8X, Formalinum 8X, 12X, 30X, 12C, 30C, 200C, 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 occasional constipation, mucous congestion, abdominal gas, headaches, fatigue, alcohol cravings, anxiety, vaginitis, rectal itching, cravings for sweets, foggy brain, mood swings, occasional diarrhea and dizziness.**

**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, 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 occasional constipation, mucous congestion, abdominal gas, headaches, fatigue, alcohol cravings, anxiety, vaginitis, rectal itching, cravings for sweets, foggy brain, mood swings, occasional diarrhea and dizziness.**

**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 43742-1285-1
HOMEOPATHIC
FNG
1 FL OZ (30 ml)

FNGFNG

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
43742-1285-12022-09-12C16284748780-19d75b9d0-6331-f424-e053-dadaa90a57ceDrug Facts:
43742-1285-12020-01-31C16284748780-19d75b9d0-6331-f424-e053-dadaa90a57ceDrug Facts:

Products#

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

DailyMed product names page 1 of 1 · 38 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43742-128543742-1285-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 34 matching rows.

Name, UNII, Kind table
NameUNIIKind
BERBERIS VULGARIS ROOT BARK1TH8Q20J0UACTIB
HORSERADISH8DS6G120HJACTIB
ECHINACEA ANGUSTIFOLIAVB06AV5US8ACTIB
LOMATIUM DISSECTUM ROOT5329928G5NACTIB
MYRRHJC71GJ1F3LACTIB
GOLDENSEALZW3Z11D0JVACTIB
PROPOLIS WAX6Y8XYV2NOFACTIB
SUS SCROFA ADRENAL GLAND398IYQ16YVACTIB
TABEBUIA IMPETIGINOSA BARK6GLA1946WXACTIB
SUS SCROFA THYMUS7B69B0BD62ACTIB
FORMALDEHYDE1HG84L3525ACTIB
IRONE1UOL152H7ACTIB
IRIDIUM44448S9773ACTIB
LYCOPODIUM CLAVATUM SPOREC88X29Y479ACTIB
PHOSPHORIC ACIDE4GA8884NNACTIB
ANEMONE PULSATILLAI76KB35JEVACTIB
SELENIUMH6241UJ22BACTIB
ZINCJ41CSQ7QDSACTIB
ADENOSINE TRIPHOSPHATE DISODIUM5L51B4DR1GACTIB
ALTERNARIA ALTERNATA52B29REC7HACTIB
ASPERGILLUS NIGER VAR. NIGER9IOA40ANG6ACTIB
CANDIDA ALBICANS4D7G21HDBCACTIB
CANDIDA PARAPSILOSIS0KZ676D44NACTIB
MUCOR RACEMOSUS17RH99LQ7GACTIB
AUREOBASIDIUM PULLULANS VAR. PULLUTANSD1A2NG69CKACTIB
RHIZOPUS STOLONIFERFEE198DK4QACTIB
SACCHAROMYCES CEREVISIAE978D8U419HACTIB
METHYLCOBALAMINBR1SN1JS2WACTIB
LACTIC ACID, L-F9S9FFU82NACTIB
STACHYBOTRYS CHARTARUMHJ4L70T1ZPACTIB
ESCHERICHIA COLI514B9K0L10ACTIB
BRUGIA MALAYIV1NN02KTF0ACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT

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
4f0abe14-7f21-4c85-842a-1b0ada66a283becd6164-2f7a-4341-8d02-67d65481f5372022-09-12WarningsExact identifier
spl id: 4f0abe14-7f21-4c85-842a-1b0ada66a283
spl set id: becd6164-2f7a-4341-8d02-67d65481f537

Reported adverse events (FAERS/openFDA)#

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