FDA.reportPublic FDA data

Symbio Myco Phlei Drops 6X

Manufacturer
Symbiopathic | Deserving Health International Corp
Effective date
2026-10-08
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
daily-update
Hydrated at
2026-10-13 04:02:46

Label at a glance#

ProductSYMBIOPATHIC
Active ingredientMYCOBACTERIUM PHLEI
Label structure10 sections

Dosage and administration

5-10 drops, three times daily.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Mycobacterium phlei 6 X

WARNINGS:

WARNINGS SECTION

If symptoms persist more than a few days, contact a licensed practitioner. As with any drug, if you are
pregnant or nursing, seek the advice of a health care professional before using this product. Keep this and all medications out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Protect from light and heat.

Tamper Evident
Do not use product if the tamper evident strip is broken
or removed from the base of the cap.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

5-10 drops, three times daily.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Purified water USP, sodium chloride

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN:In case of overdose, get medical help or call a Poison Control Center right away.

INDICATIONS:

INDICATIONS & USAGE SECTION

Acts as a strong immune modulator in conditions of the respiratory tract, extra pulmonary tuberculosis and lungs.
Also for fever and conditions of weakness.

PURPOSE:

OTC - PURPOSE SECTION

For internal indications according to traditional homeopathic practice.

OTHER INFORMATION:

SPL UNCLASSIFIED SECTION

Protect from light and heat.

For professional distribution only.

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

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label 10MlLabel 10Ml

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69710-25569710-255-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
MYCOBACTERIUM PHLEIT67520T45FACTIB
SODIUM CHLORIDE451W47IQ8XIACT
WATER059QF0KO0RIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
32025-10-11full-release2026-06-01 02:37:06
22024-12-11full-release2026-06-01 02:29:30

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
40e5ceff-390a-a297-e063-6394a90af1242904c6e1-2c54-8035-e063-6294a90aa04b2025-10-11WarningsExact identifier
spl set id: 2904c6e1-2c54-8035-e063-6294a90aa04b

Reported adverse events (FAERS/openFDA)#

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