FDA.reportPublic FDA data

PARA-ROQUEFORTI 4X

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 04:02:10

Label at a glance#

ProductSYMBIO PARA/ROQUEFORTI DROPS
Active ingredientPENICILLIUM ROQUEFORTI, CANDIDA PARAPSILOSIS
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

Candida Parapsilosis 4X
Penicillium Roqueforti 4X

WARNINGS:

WARNINGS SECTION

Do not useif 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 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

This remedy is indicated for symptoms associated with yeast infections and intestinal dysbacteria 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

Para-Roqueforti 4XPara-Roqueforti 4X

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
f1e0dc7e-7d61-4625-b6d9-4894927679d7Product name220211025
e4870509-7e28-6f92-f0be-dd3dd889a9cfProduct name520200810
6e9d4a47-c464-b93e-aebc-ad7bffc9c4cdProduct name220190619
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
5668b646-cd56-c3c7-bdea-3f6b1a8840dbProduct name120140508
684ea482-2e8b-14af-5664-b98f1e402036Product name120140508
810ab97e-f109-f41c-7c83-6a652a9cbf43Product name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
b060cc1a-fe47-856b-0b77-4448b5963de8Product name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69710-165-112024-12-11C16284748780-11030e365-4bfa-111a-e063-dadaa90a10e2PARA-ROQUEFORTI 4X
69710-165-112024-12-11C16284748780-11030e365-4bfa-111a-e063-dadaa90a10e2PARA-ROQUEFORTI 4X
69710-165-112024-12-11C16284748780-11030e365-4bfa-111a-e063-dadaa90a10e2PARA-ROQUEFORTI 4X
69710-165-112024-07-30C16284748780-11030e365-4bfa-111a-e063-dadaa90a10e2PARA-ROQUEFORTI 4X
69710-165-112024-07-30C16284748780-11030e365-4bfa-111a-e063-dadaa90a10e2PARA-ROQUEFORTI 4X
69710-165-112024-07-30C16284748780-11030e365-4bfa-111a-e063-dadaa90a10e2PARA-ROQUEFORTI 4X
69710-165-112024-01-30C16284748780-11030e365-4bfa-111a-e063-dadaa90a10e2PARA-ROQUEFORTI 4X
69710-165-112024-01-30C16284748780-11030e365-4bfa-111a-e063-dadaa90a10e2PARA-ROQUEFORTI 4X
69710-165-112024-01-30C16284748780-11030e365-4bfa-111a-e063-dadaa90a10e2PARA-ROQUEFORTI 4X

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69710-16569710-165-11

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
PENICILLIUM ROQUEFORTI7ORP6R724LACTIB
CANDIDA PARAPSILOSIS0KZ676D44NACTIB
WATER059QF0KO0RIACT
SODIUM CHLORIDE451W47IQ8XIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
32025-10-11full-release2026-06-01 02:37:05
22024-12-11full-release2026-06-01 02:29:28

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
40e5e3bf-76fa-7552-e063-6294a90af7680788c3b6-d876-b337-e063-6294a90acd3a2025-10-11WarningsExact identifier
spl set id: 0788c3b6-d876-b337-e063-6294a90acd3a

Reported adverse events (FAERS/openFDA)#

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