FDA.reportPublic FDA data

CEREBRINUM

Manufacturer
Seroyal USA | SAN'UP
Effective date
2022-11-07
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:49:27

Label at a glance#

ProductCEREBRINUM
Active ingredientORYCTOLAGUS CUNICULUS HYPOTHALAMUS
Label structure11 sections

Label contents#

Full prescribing information#

Formula

OTC - ACTIVE INGREDIENT SECTION

Each Drop Contains: Oryctolagus cuniculus
(Rabbit) Brain 4CH

Indications

OTC - PURPOSE SECTION

Helps support mental alertness and overall
mental health.

Warnings

WARNINGS SECTION

Stop use and ask a doctor if symptoms persist or worsen.
If pregnant or breastfeeding, ask a health professional
before use. Keep out of reach of children. In case of
overdose, get medical help or contact a Poison Control Center
right away

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breastfeeding, ask a health professional
before use.

OTC - STOP USE SECTION

If symptoms persist or worsen, consult your healthcare practitioner.

OVERDOSAGE SECTION

In case of overdose, get medical help or contact a Poison Control Center right away.

INACTIVE INGREDIENT SECTION

Inactive ingredients: Ethanol (beet), purified water

DOSAGE & ADMINISTRATION SECTION

Adults and Children (over 12 years): Take 10 drops two to three times daily

Children (1-12 years): Take three to five drops two to three times daily Take for three weeks, then one week off and three weeks on for three months or as recommended by your healthcare practitioner. Evaluate after three months.

Indications

INDICATIONS & USAGE SECTION

Helps support mental alertness and overall mental health.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 62106-0247-0
CEREBRINUM
4CH
Homeopathic
Remedy
Contains
30% Alcohol
1 fl oz (30 ml)

62106-0247-062106-0247-0

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
62106-024762106-0247-0

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
ORYCTOLAGUS CUNICULUS HYPOTHALAMUSQMH532G890ACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT

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
06485770-ff2c-aa7c-e063-6294a90a0b987d3e8360-842c-9c38-e053-2991aa0adb132023-09-26WarningsExact identifier
spl set id: 7d3e8360-842c-9c38-e053-2991aa0adb13

Reported adverse events (FAERS/openFDA)#

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