FDA.reportPublic FDA data

Cerebromax

Manufacturer
Deseret Biologicals, Inc. | Apotheca Company
Effective date
2019-02-06
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 00:31:40

Label at a glance#

ProductCerebromax
Active ingredientACETYLCHOLINE CHLORIDE, OCTOPAMINE HYDROCHLORIDE, TAURINE, ADENOSINE CYCLIC PHOSPHATE, SUS SCROFA CEREBRUM, SUS SCROFA DIENCEPHALON, SUS SCROFA PINEAL GLAND, SUS SCROFA THALAMUS LATERAL GENICULATE NUCLEUS, EPINEPHRINE, DOPAMINE HYDROCHLORIDE, .GAMMA.-AMINOBUTYRIC ACID, NOREPINEPHRINE, SEROTONIN HYDROCHLORIDE
Label structure9 sections

Dosage and administration

3-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Acetylcholine Chloride 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Octopamine (Hydrochloride) 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Taurine 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Adenosinum Cyclophosphoricum 8X, Cerebrum Suis 8X, Diencephalon (Suis) 8X, Pineal Gland (Suis) 8X, Thalamus Opticus (Suis) 8X, Adrenalinum 8X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Dopamine Hydrochloride 8X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, GABA (Gamma-Aminobutyric Acid) 8X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Norepinephrine 8X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Serotonin (Hydrochloride) 8X, 12X, 30X, 200X, 12C, 30C, 60C, 200C.

HOMEOPATHIC INDICATIONS:

OTC - PURPOSE SECTION

For the temporary relief of symptoms relating to sleep, memory, and emotional issues.**

**These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

WARNINGS:

WARNINGS SECTION

Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away.

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

Tamper seal: "Sealed for Your protection." Do not use if seal is broken or missing.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

3-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

HOMEOPATHIC INDICATIONS:

INDICATIONS & USAGE SECTION

For the temporary relief of symptoms relating to sleep, memory, and emotional issues.**

**These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized Water, 25% Ethanol

QUESTIONS:

OTC - QUESTIONS SECTION

Dist. By: Deseret Biologicals, Inc.

469 W. Parkland Drive

Sandy, UT 84070 www.desbio.com

PACKAGE DISPLAY LABEL:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DESBIO

NDC 43742-1269-1

HOMEOPATHIC

CEREBROMAX

1 FL OZ (30 ml)

CerebromaxCerebromax

Products#

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

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43742-126943742-1269-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
ACETYLCHOLINE CHLORIDEAF73293C2RACTIB
OCTOPAMINE HYDROCHLORIDE37YAS5L9HQACTIB
TAURINE1EQV5MLY3DACTIB
ADENOSINE CYCLIC PHOSPHATEE0399OZS9NACTIB
SUS SCROFA CEREBRUM4GB5DQR532ACTIB
SUS SCROFA DIENCEPHALON23PJ4252VLACTIB
SUS SCROFA PINEAL GLAND050QZ2EDK7ACTIB
SUS SCROFA THALAMUS LATERAL GENICULATE NUCLEUSP146I3107TACTIB
EPINEPHRINEYKH834O4BHACTIB
DOPAMINE HYDROCHLORIDE7L3E358N9LACTIB
.GAMMA.-AMINOBUTYRIC ACID2ACZ6IPC6IACTIB
NOREPINEPHRINEX4W3ENH1CVACTIB
SEROTONIN HYDROCHLORIDEGKN429M9VSACTIB
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
7cc2ef1e-cdb2-41d4-a80d-e922b7bdba57750dbe72-0eb7-4bbd-8d59-312b6f5dc17a2019-02-06WarningsExact identifier
spl id: 7cc2ef1e-cdb2-41d4-a80d-e922b7bdba57
spl set id: 750dbe72-0eb7-4bbd-8d59-312b6f5dc17a

Reported adverse events (FAERS/openFDA)#

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