FDA.reportPublic FDA data

Mytox

Manufacturer
Professional Complementary Health Formulas | Natural Pharmaceutical Manufacturing LLC
Effective date
2026-01-08
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
monthly-update
Hydrated at
2026-06-03 17:49:32

Label at a glance#

ProductMytox 6021
Active ingredientSODIUM BORATE, COLCHICUM AUTUMNALE BULB, AMANITA MUSCARIA FRUITING BODY, ARSENIC TRIOXIDE, DROSERA ROTUNDIFOLIA WHOLE, BUFO BUFO CUTANEOUS GLAND, UBIDECARENONE
Label structure9 sections

Dosage and administration

Place drops under tongue 30 minutes before/after meals. Adults and children 12 years and over: Take 10 drops up to 3 times per day. Consult a physician for use in children under 12 years of age.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Borax 4X
Colchicum autumnale 4X
Agaricus muscarius 6X
Arsenicum album 6X
Drosera rotundifolia 6X
Bufo rana 8X
Coenzyme Q10 12X

QUESTIONS

OTC - QUESTIONS SECTION

Professional Formulas

PO Box 2034 Lake Oswego, OR 97035

INDICATIONS

INDICATIONS & USAGE SECTION

For the temporary relief of red or itchy skin, cough, joint or muscle pain or stiffness, shortness of breath, sneezing, occasional headache, dizziness, or fatigue.*

OTC - PURPOSE SECTION

*Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

WARNINGS

WARNINGS SECTION

Persistent symptoms may be a sign of a serious condition. If symptoms persist or are accompanied by a fever, rash, or persistent headache, consult a doctor. Keep out of the reach of children. In case of overdose, get medical help or contact a poison control center right away. If pregnant or breastfeeding, ask a healthcare professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breastfeeding, ask a healthcare professional before use.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Place drops under tongue 30 minutes before/after meals. Adults and children 12 years and over: Take 10 drops up to 3 times per day. Consult a physician for use in children under 12 years of age.

OTHER INFORMATION

OTHER SAFETY INFORMATION

Tamper resistant. If seal is broken, do not use. After opening, close container tightly and store at room temperature away from heat.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

20% ethanol, purified water.

LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Est 1985

Professional Formulas

Complementary Health

Mytox

Homeopathic Remedy

2 FL. OZ. (59 mL)

Label imageLabel image

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
63f39a63-5cd1-4016-bd86-2bbb0f6c3139Product name320240506
e5a77e9c-c528-733a-173d-914a234c024bProduct name520240506

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63083-6021-22026-01-09C16284748780-11030e365-2309-111a-e063-dadaa90a10e2X21
63083-6021-22026-01-09C16284748780-11030e365-2309-111a-e063-dadaa90a10e2X21
63083-6021-22024-01-30C16284748780-11030e365-2309-111a-e063-dadaa90a10e2X21
63083-6021-22024-01-30C16284748780-11030e365-2309-111a-e063-dadaa90a10e2X21

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63083-6021-2Mytox602159 mL in 1 BOTTLE, DROPPERLIQUID592

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63083-602163083-6021-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
SODIUM BORATE91MBZ8H3QOACTIB
COLCHICUM AUTUMNALE BULB993QHL78E6ACTIB
AMANITA MUSCARIA FRUITING BODYDIF093I037ACTIB
ARSENIC TRIOXIDES7V92P67HOACTIB
DROSERA ROTUNDIFOLIA WHOLEQR44N9XPJQACTIB
BUFO BUFO CUTANEOUS GLANDQ59QU6N72QACTIB
UBIDECARENONEEJ27X76M46ACTIB
ALCOHOL3K9958V90MIACT
WATER059QF0KO0RIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12019-08-15full-release2026-06-01 02:17:15

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
Mytox 6021MYTOXProfessional Complementary Health Formulasbc89020f-c089-4351-a700-0ed19ec816042026-01-08WarningsExact identifier
ndc (package): 63083-6021-2
ndc (product): 63083-6021
ndc11 (package): 63083602102
spl id: f48bbd72-9f6f-4aa4-8777-d02e3830d7c6
spl set id: bc89020f-c089-4351-a700-0ed19ec81604

Reported adverse events (FAERS/openFDA)#

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