FDA.reportPublic FDA data

Asper 4X

Manufacturer
Symbiopathic | Deserving Health International Corp
Effective date
2026-10-08
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
daily-update
Hydrated at
2026-10-13 04:02:29

Label at a glance#

ProductSYMBIO ASPER DROPS
Active ingredientASPERGILLUS NIGER VAR. NIGER
Label structure12 sections

Dosage and administration

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

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Aspergillus Niger 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 or as directed.

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 allergies, rheumatic illnesses, stomach ulcers, hyperactive thyroid, lymphatic problems, and phthisis 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

AsperAsper

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
69710-10569710-105-11

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
ASPERGILLUS NIGER VAR. NIGER9IOA40ANG6ACTIB
WATER059QF0KO0RIACT
SODIUM CHLORIDE451W47IQ8XIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
42025-10-11full-release2026-06-01 02:37:06
32024-12-11full-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
40e5c633-014e-582e-e063-6294a90a3c2e29047913-5048-9678-e063-6394a90a23892025-10-11WarningsExact identifier
spl set id: 29047913-5048-9678-e063-6394a90a2389

Reported adverse events (FAERS/openFDA)#

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