MYCCombination

Manufacturer
Deseret Biologicals, Inc. | Apotheca Company
Effective date
2023-12-04
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:24:58

Label at a glance#

ProductMYCCombination
Active ingredientONION, ECHINACEA ANGUSTIFOLIA WHOLE, SODIUM SULFATE, POTASSIUM CARBONATE, MEPHITIS MEPHITIS ANAL GLAND FLUID, SANGUINARIA CANADENSIS ROOT, BLATTA ORIENTALIS, AMANITA MUSCARIA FRUITING BODY, ANTIMONY POTASSIUM TARTRATE, ARSENIC TRIIODIDE, PHENOL, CINCHONA OFFICINALIS BARK, IRON, PHYTOLACCA AMERICANA ROOT, CLAVICEPS PURPUREA SCLEROTIUM, SULFURIC ACID, THUJA OCCIDENTALIS LEAFY TWIG, AMMONIUM CARBONATE, ASPERGILLUS NIGER VAR. NIGER
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

Allium Cepa 6X, Echinacea (Angustifolia) 6X, Natrum Sulphuricum 6X, 12X, 30X, Kali Carbonicum 8X, Mephitis Mephitica 8X, Sanguinaria Canadensis 8X, Blatta Orientalis 8X, 12X, 30X, Agaricus Muscarius 12X, Antimonium Tartaricum 12X, Arsenicum Iodatum 12X, Carbolicum Acidum 12X, Cinchona Officinalis 12X, Ferrum Metallicum 12X, Phytolacca Decandra 12X, Secale Cornutum 12X, Sulphuricum Acidum 12X, Thuja Occidentalis 12X, Ammonium Carbonicum 12X, 24X, 30X, Aspergillus Niger 15X, 30X, 60X, 100X, 200X.

HOMEOPATHIC INDICATIONS:

OTC - PURPOSE SECTION

For the temporary relief of symptoms of mold toxicity and illness including coughing, wheezing, burning in throat, headache, fatigue, and joint pain.**

**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

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 the temporary relief of symptoms of mold toxicity and illness including coughing, wheezing, burning in throat, headache, fatigue, and joint pain.**

**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

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DESBIO
NDC 43742-1934-1
HOMEOPATHIC
MYC:Combination
1 FL OZ (30 ml)

MYC:CombinationMYC:Combination

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
95250459-30e4-45c1-b08a-993044f49109Product name220250805
63f39a63-5cd1-4016-bd86-2bbb0f6c3139Product name320240506
e5a77e9c-c528-733a-173d-914a234c024bProduct name520240506
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
910c1bd7-67d1-44c7-ad4f-9445f827edccProduct name120230808
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43742-1934-1MYCCombination30 mL in 1 BOTTLE, DROPPERLIQUID303

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43742-1934MYCCOMBINATION (ALLIUM CEPA, ECHINACEA (ECHINACEA ANGUSTIFOLIA), NATRUM SULPHURICUM, KALI CARBONICUM, MEPHITIS MEPHITICA, SANGUINARIA CANADENSIS, BLATTA ORIENTALIS, AGARICUS MUSCARIUS, ANTIMONIUM TARTARICUM, ARSENICUM IODATUM, CARBOLICUM ACIDUM, CINCHONA OFFICINALIS, FERRUM METALLICUM, PHYTOLACCA DECANDRA, SECALE CORNUTUM, SULPHURICUM ACIDUM, THUJA OCCIDENTALIS, AMMONIUM CARBONICUM, ASPERGILLUS NIGER) LIQUID [DESERET BIOLOGICALS, INC.]3Current NDC, Legacy NDC, 1 package rows20231205_795c34c6-71c8-4c36-b441-4bca55a43575.zip

Products#

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

DailyMed product names page 1 of 1 · 29 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43742-193443742-1934-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 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
MYCCombinationALLIUM CEPA, ECHINACEA (ECHINACEA ANGUSTIFOLIA), NATRUM SULPHURICUM, KALI CARBONICUM, MEPHITIS MEPHITICA, SANGUINARIA CANADENSIS, BLATTA ORIENTALIS, AGARICUS MUSCARIUS, ANTIMONIUM TARTARICUM, ARSENICUM IODATUM, CARBOLICUM ACIDUM, CINCHONA OFFICINALIS, FERRUM METALLICUM, PHYTOLACCA DECANDRA, SECALE CORNUTUM, SULPHURICUM ACIDUM, THUJA OCCIDENTALIS, AMMONIUM CARBONICUM, ASPERGILLUS NIGERDeseret Biologicals, Inc.795c34c6-71c8-4c36-b441-4bca55a435752023-12-04WarningsExact identifier
ndc (package): 43742-1934-1
ndc (product): 43742-1934
ndc11 (package): 43742193401
spl id: b1db4354-95ca-4b26-a46f-69e8b47fd8a7
spl set id: 795c34c6-71c8-4c36-b441-4bca55a43575

Reported adverse events (FAERS/openFDA)#

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