FDA.reportPublic FDA data

SYMBIO MUC EYE DROPS

Manufacturer
Symbiopathic | Biological Health Group Corporation
Effective date
2023-05-15
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:21:11

Label at a glance#

ProductSYMBIO MUC EYE DROPS
Active ingredientMUCOR RACEMOSUS
Label structure12 sections

Dosage and administration

Put 1 – 2 drops in affected eye(s), twice daily.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Mucor racemosus 5X

WARNINGS:

WARNINGS SECTION

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

• Contact lens wearers consult physician prior to using.

• To avoid contamination – do not touch tip to any surface.

• Replace cap after every use. • Use within 30 days of opening.

• EXPIRATION DATE ONLY REFERS TO THE UNOPENED BOTTLE.

• The use of this container by more than one person may spread infection.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Put 1 – 2 drops in affected eye(s), twice daily.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Purified water, 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

This remedy is indicated for red and irritated eyes, dry eyes, and allergy eyes with burning and itching according to traditional homeopathic practice.*

PURPOSE:

OTC - PURPOSE SECTION

Irritated eyes.*

If pregnant or breast feeding...

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast feeding, ask a health professional before use.

ASK DOCTOR:

OTC - ASK DOCTOR SECTION

Consult a physician if symptoms worsen or last for more than 7 days.

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

Muc EyeMuc Eye

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69711-125-612024-07-30C16284748780-19d75b9d0-78a3-f424-e053-dadaa90a57cemuc 5x
69711-125-612024-01-30C16284748780-19d75b9d0-78a3-f424-e053-dadaa90a57cemuc 5x
69711-125-612023-05-15C16284748780-19d75b9d0-78a3-f424-e053-dadaa90a57cemuc 5x
69711-125-612022-01-28C16284748780-19d75b9d0-78a3-f424-e053-dadaa90a57cemuc 5x
69711-125-612020-03-26C16284748780-19d75b9d0-78a3-f424-e053-dadaa90a57cemuc 5x
69711-125-612020-01-31C16284748780-19d75b9d0-78a3-f424-e053-dadaa90a57cemuc 5x

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69711-125-61SYMBIO MUC EYE DROPS1 in 1 CARTONLIQUID13
69711-125-61SYMBIO MUC EYE DROPS5 mL in 1 BOTTLELIQUID53

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69711-125SYMBIO MUC EYE DROPS (MUCOR RACEMOSUS) LIQUID [SYMBIOPATHIC]3Legacy NDC, 2 package rows20230516_3c57eca8-96b0-2bad-e054-00144ff8d46c.zip

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
69711-12569711-125-61

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
SODIUM CHLORIDE451W47IQ8XIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7IACT
MUCOR RACEMOSUS17RH99LQ7GACTIB

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
fbbe5a98-d573-4c1f-e053-6294a90a51f13c57eca8-96b0-2bad-e054-00144ff8d46c2023-05-15WarningsExact identifier
spl id: fbbe5a98-d573-4c1f-e053-6294a90a51f1
spl set id: 3c57eca8-96b0-2bad-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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