FDA.reportPublic FDA data

SYMBIO QUENT 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 QUENT DROPS
Active ingredientPENICILLIUM GLABRUM
Label structure12 sections

Dosage and administration

Take 5 – 10 drops orally, three times per day.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Penicillium frequentans 4X

WARNINGS:

WARNINGS SECTION

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

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Take 5 – 10 drops orally, three times per day.

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 symptoms associated with colds; flu, inflamed nasal passages, pre- and post- influenza neuralgia, laryngitis, sinusitis and myalgias according to traditional homeopathic practice.*

PURPOSE:

OTC - PURPOSE SECTION

For internal indications according to traditional homeopathic practice.

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

Quent 4XQuent 4X

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69711-175-112024-07-30C16284748780-19d75b9cf-f467-f424-e053-dadaa90a57ceQuent 4X
69711-175-112024-01-30C16284748780-19d75b9cf-f467-f424-e053-dadaa90a57ceQuent 4X
69711-175-112023-05-15C16284748780-19d75b9cf-f467-f424-e053-dadaa90a57ceQuent 4X
69711-175-112022-01-28C16284748780-19d75b9cf-f467-f424-e053-dadaa90a57ceQuent 4X
69711-175-112020-03-26C16284748780-19d75b9cf-f467-f424-e053-dadaa90a57ceQuent 4X
69711-175-112020-01-31C16284748780-19d75b9cf-f467-f424-e053-dadaa90a57ceQuent 4X

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69711-175-11SYMBIO QUENT DROPS10 mL in 1 BOTTLELIQUID103
69711-175-11SYMBIO QUENT DROPS1 in 1 CARTONLIQUID13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69711-175SYMBIO QUENT DROPS (PENICILLIUM FREQUENTANS) LIQUID [SYMBIOPATHIC]3Legacy NDC, 2 package rows20230516_3c574708-24d7-0465-e054-00144ff88e88.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
69711-17569711-175-11

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
SODIUM CHLORIDE451W47IQ8XIACT
WATER059QF0KO0RIACT
PENICILLIUM GLABRUM2IN23YUE0IACTIB

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
fbbfbed5-fa9e-c901-e053-6394a90a32393c574708-24d7-0465-e054-00144ff88e882023-05-15WarningsExact identifier
spl id: fbbfbed5-fa9e-c901-e053-6394a90a3239
spl set id: 3c574708-24d7-0465-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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